Sodium hypochlorite: Difference between revisions
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{{ | {{DrugProjectFormSinglePage | ||
| | |authorTag={{DB}} | ||
|genericName=Sodium hypochlorite | |||
|aOrAn=an | |||
|drugClass=anti- infective agent | |||
|indicationType=treatment | |||
|indication=infection of the skin and tissue | |||
|adverseReactions=<!--Black Box Warning--> | |||
|blackBoxWarningTitle=<span style="color:#FF0000;">ConditionName: </span> | |||
|blackBoxWarningBody=<i><span style="color:#FF0000;">ConditionName: </span></i> | |||
* Content | |||
| | |||
| | <!--Adult Indications and Dosage--> | ||
| | |||
| | |||
| | |||
| | |||
| | |||
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<!--FDA-Labeled Indications and Dosage (Adult)--> | |||
|fdaLIADAdult======Infection of the skin and tissue===== | |||
* To prevent and treat infection of the skin and tissue. | |||
* Pre and post surgery- Cuts, abrasions and skin ulcers | |||
* Dosing Information | |||
:*Pour on or apply to affected area. For wound management, use as an irrigant, cleanser, or the wetting agent for a wet-to-moist dressing. Apply once daily for lightly to moderately exudative wounds. Apply twice daily for highly exudative or highly contaminated wounds. Protect surrounding intact skin with a moisture barrier ointment or skin sealant as needed. | |||
<!--Off-Label Use and Dosage (Adult)--> | |||
== | <!--Guideline-Supported Use (Adult)--> | ||
|offLabelAdultGuideSupport=*There is limited information regarding <i>Off-Label Guideline-Supported Use</i> of Sodium hypochlorite in adult patients. | |||
|offLabelAdultNoGuideSupport=*There is limited information regarding <i>Off-Label Non–Guideline-Supported Use</i> of Sodium hypochlorite in adult patients. | |||
|offLabelPedGuideSupport=*There is limited information regarding <i>Off-Label Guideline-Supported Use</i> of Sodium hypochlorite in pediatric patients. | |||
|offLabelPedNoGuideSupport=*There is limited information regarding <i>Off-Label Non–Guideline-Supported Use</i> of Sodium hypochlorite in pediatric patients. | |||
|warnings=* For external use only. | |||
* Stop use and ask a doctor if redness, irritation, swelling or pain persists or increases. | |||
*Do not use if sensitive to chlorine compounds. | |||
*Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. | |||
|drugInteractions=<!--Use in Specific Populations--> | |||
|useInPregnancyFDA=* '''Pregnancy Category''' | |||
|useInPregnancyAUS=* '''Australian Drug Evaluation Committee (ADEC) Pregnancy Category''' | |||
*There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of {{PAGENAME}} in women who are pregnant. | |||
|useInLaborDelivery=*There is no FDA guidance on use of {{PAGENAME}} during labor and delivery. | |||
|useInNursing=*There is no FDA guidance on the use of {{PAGENAME}} with respect to nursing mothers. | |||
|useInPed=*There is no FDA guidance on the use of {{PAGENAME}} with respect to pediatric patients. | |||
|useInGeri=*There is no FDA guidance on the use of {{PAGENAME}} with respect to geriatric patients. | |||
|useInGender=*There is no FDA guidance on the use of {{PAGENAME}} with respect to specific gender populations. | |||
|useInRace=*There is no FDA guidance on the use of {{PAGENAME}} with respect to specific racial populations. | |||
|useInRenalImpair=*There is no FDA guidance on the use of {{PAGENAME}} in patients with renal impairment. | |||
|useInHepaticImpair=*There is no FDA guidance on the use of {{PAGENAME}} in patients with hepatic impairment. | |||
|useInReproPotential=*There is no FDA guidance on the use of {{PAGENAME}} in women of reproductive potentials and males. | |||
|useInImmunocomp=*There is no FDA guidance one the use of {{PAGENAME}} in patients who are immunocompromised. | |||
<!--Administration and Monitoring--> | |||
|administration='''Directions''' | |||
* Pour on or apply to affected area. For wound management, use as an irrigant, cleanser, or the wetting agent for a wet-to-moist dressing. Apply once daily for lightly to moderately exudative wounds. Apply twice daily for highly exudative or highly contaminated wounds. Protect surrounding intact skin with a moisture barrier ointment or skin sealant as needed. | |||
|monitoring=*There is limited information regarding <i>Monitoring</i> of {{PAGENAME}} in the drug label. | |||
<!--IV Compatibility--> | |||
|IVCompat=*There is limited information regarding <i>IV Compatibility</i> of {{PAGENAME}} in the drug label. | |||
<!--Overdosage--> | |||
|drugBox=[[File:Sodium hypochlorite wiki.png|600px|thumbnail|left]] | |||
{{clear}} | |||
|PD=*There is limited information regarding <i>Pharmacodynamics</i> of {{PAGENAME}} in the drug label. | |||
<!--Pharmacokinetics--> | |||
|PK=*There is limited information regarding <i>Pharmacokinetics</i> of {{PAGENAME}} in the drug label. | |||
<!--Nonclinical Toxicology--> | |||
|nonClinToxic=*There is limited information regarding <i>Nonclinical Toxicology</i> of {{PAGENAME}} in the drug label. | |||
<!--Clinical Studies--> | |||
|clinicalStudies=*There is limited information regarding <i>Clinical Studies</i> of {{PAGENAME}} in the drug label. | |||
<!--How Supplied--> | |||
|howSupplied=* | |||
<!--Patient Counseling Information--> | |||
|storage=* Store at room temperature. | |||
* May bleach clothing. | |||
= | * Keep container closed when not using. | ||
[[ | |packLabel=[[File:Sodium hypochlorite pdp.jpg|600px|thumbnail|left]] | ||
{{clear}} | |||
[[File:Sodium hypochlorite label.png|600px|thumbnail|left]] | |||
Sodium hypochlorite | {{clear}} | ||
|fdaPatientInfo=*There is limited information regarding <i>Patient Counseling Information</i> of {{PAGENAME}} in the drug label. | |||
<!--Precautions with Alcohol--> | |||
|alcohol=* Alcohol-{{PAGENAME}} interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication. | |||
<!--Brand Names--> | |||
|brandNames=* ®<ref>{{Cite web | title = | url = }}</ref> | |||
<!--Look-Alike Drug Names--> | |||
|lookAlike=* A® — B®<ref name="www.ismp.org">{{Cite web | last = | first = | title = http://www.ismp.org | url = http://www.ismp.org | publisher = | date = }}</ref> | |||
<!--Drug Shortage Status--> | |||
|drugShortage= | |||
}} | |||
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{{LabelImage | |||
|fileName={{PAGENAME}}11.png | |||
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<!--Pill Image--> | |||
<!--Label Display Image--> | |||
<!--Category--> | |||
[[ | [[Category:Drug]] | ||
Latest revision as of 15:39, 11 December 2014
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Deepika Beereddy, MBBS [2]
Disclaimer
WikiDoc MAKES NO GUARANTEE OF VALIDITY. WikiDoc is not a professional health care provider, nor is it a suitable replacement for a licensed healthcare provider. WikiDoc is intended to be an educational tool, not a tool for any form of healthcare delivery. The educational content on WikiDoc drug pages is based upon the FDA package insert, National Library of Medicine content and practice guidelines / consensus statements. WikiDoc does not promote the administration of any medication or device that is not consistent with its labeling. Please read our full disclaimer here.
Overview
Sodium hypochlorite is an anti- infective agent that is FDA approved for the treatment of infection of the skin and tissue. Common adverse reactions include .
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
Infection of the skin and tissue
- To prevent and treat infection of the skin and tissue.
- Pre and post surgery- Cuts, abrasions and skin ulcers
- Dosing Information
- Pour on or apply to affected area. For wound management, use as an irrigant, cleanser, or the wetting agent for a wet-to-moist dressing. Apply once daily for lightly to moderately exudative wounds. Apply twice daily for highly exudative or highly contaminated wounds. Protect surrounding intact skin with a moisture barrier ointment or skin sealant as needed.
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
- There is limited information regarding Off-Label Guideline-Supported Use of Sodium hypochlorite in adult patients.
Non–Guideline-Supported Use
- There is limited information regarding Off-Label Non–Guideline-Supported Use of Sodium hypochlorite in adult patients.
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
There is limited information regarding Sodium hypochlorite FDA-Labeled Indications and Dosage (Pediatric) in the drug label.
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
- There is limited information regarding Off-Label Guideline-Supported Use of Sodium hypochlorite in pediatric patients.
Non–Guideline-Supported Use
- There is limited information regarding Off-Label Non–Guideline-Supported Use of Sodium hypochlorite in pediatric patients.
Contraindications
There is limited information regarding Sodium hypochlorite Contraindications in the drug label.
Warnings
- For external use only.
- Stop use and ask a doctor if redness, irritation, swelling or pain persists or increases.
- Do not use if sensitive to chlorine compounds.
- Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Sodium hypochlorite Clinical Trials Experience in the drug label.
Postmarketing Experience
There is limited information regarding Sodium hypochlorite Postmarketing Experience in the drug label.
Drug Interactions
There is limited information regarding Sodium hypochlorite Drug Interactions in the drug label.
Use in Specific Populations
Pregnancy
- Pregnancy Category
- Australian Drug Evaluation Committee (ADEC) Pregnancy Category
- There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Sodium hypochlorite in women who are pregnant.
Labor and Delivery
- There is no FDA guidance on use of Sodium hypochlorite during labor and delivery.
Nursing Mothers
- There is no FDA guidance on the use of Sodium hypochlorite with respect to nursing mothers.
Pediatric Use
- There is no FDA guidance on the use of Sodium hypochlorite with respect to pediatric patients.
Geriatic Use
- There is no FDA guidance on the use of Sodium hypochlorite with respect to geriatric patients.
Gender
- There is no FDA guidance on the use of Sodium hypochlorite with respect to specific gender populations.
Race
- There is no FDA guidance on the use of Sodium hypochlorite with respect to specific racial populations.
Renal Impairment
- There is no FDA guidance on the use of Sodium hypochlorite in patients with renal impairment.
Hepatic Impairment
- There is no FDA guidance on the use of Sodium hypochlorite in patients with hepatic impairment.
Females of Reproductive Potential and Males
- There is no FDA guidance on the use of Sodium hypochlorite in women of reproductive potentials and males.
Immunocompromised Patients
- There is no FDA guidance one the use of Sodium hypochlorite in patients who are immunocompromised.
Administration and Monitoring
Administration
Directions
- Pour on or apply to affected area. For wound management, use as an irrigant, cleanser, or the wetting agent for a wet-to-moist dressing. Apply once daily for lightly to moderately exudative wounds. Apply twice daily for highly exudative or highly contaminated wounds. Protect surrounding intact skin with a moisture barrier ointment or skin sealant as needed.
Monitoring
- There is limited information regarding Monitoring of Sodium hypochlorite in the drug label.
IV Compatibility
- There is limited information regarding IV Compatibility of Sodium hypochlorite in the drug label.
Overdosage
There is limited information regarding Sodium hypochlorite overdosage. If you suspect drug poisoning or overdose, please contact the National Poison Help hotline (1-800-222-1222) immediately.
Pharmacology
Mechanism of Action
There is limited information regarding Sodium hypochlorite Mechanism of Action in the drug label.
Structure
There is limited information regarding Sodium hypochlorite Structure in the drug label.
Pharmacodynamics
- There is limited information regarding Pharmacodynamics of Sodium hypochlorite in the drug label.
Pharmacokinetics
- There is limited information regarding Pharmacokinetics of Sodium hypochlorite in the drug label.
Nonclinical Toxicology
- There is limited information regarding Nonclinical Toxicology of Sodium hypochlorite in the drug label.
Clinical Studies
- There is limited information regarding Clinical Studies of Sodium hypochlorite in the drug label.
How Supplied
Storage
- Store at room temperature.
- May bleach clothing.
- Keep container closed when not using.
Images
Drug Images
{{#ask: Page Name::Sodium hypochlorite |?Pill Name |?Drug Name |?Pill Ingred |?Pill Imprint |?Pill Dosage |?Pill Color |?Pill Shape |?Pill Size (mm) |?Pill Scoring |?NDC |?Drug Author |format=template |template=DrugPageImages |mainlabel=- |sort=Pill Name }}
Package and Label Display Panel
{{#ask: Label Page::Sodium hypochlorite |?Label Name |format=template |template=DrugLabelImages |mainlabel=- |sort=Label Page }}
Patient Counseling Information
- There is limited information regarding Patient Counseling Information of Sodium hypochlorite in the drug label.
Precautions with Alcohol
- Alcohol-Sodium hypochlorite interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.
Brand Names
- ®[1]
Look-Alike Drug Names
- A® — B®[2]
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.
- ↑ Empty citation (help)
- ↑ "http://www.ismp.org". External link in
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(help)
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