Hexachlorophene
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Alberto Plate [2]
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Overview
Hexachlorophene is an antibacterial cleansing agent that is FDA approved for the procedure of surgical scrubing and a bacteriostatic skin cleanser. It may also be used to control an outbreak of gram-positive infection where other infection control procedures have been unsuccessful. Use only as long as necessary for infection control. Common adverse reactions include dermatitis, photosensitivity.
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
There is limited information regarding Hexachlorophene FDA-Labeled Indications and Dosage (Adult) in the drug label.
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of Hexachlorophene in adult patients.
Non–Guideline-Supported Use
There is limited information regarding Off-Label Non–Guideline-Supported Use of Hexachlorophene in adult patients.
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
There is limited information regarding Hexachlorophene 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 Hexachlorophene in pediatric patients.
Non–Guideline-Supported Use
There is limited information regarding Off-Label Non–Guideline-Supported Use of Hexachlorophene in pediatric patients.
Contraindications
- pHisoHex must not be used on burned or denuded skin.
- pHisoHex must not be used for bathing infants. Infants may absorb the active compound in pHisoHex more readily than older children and adults. Such absorption has been associated with central nervous system effects such as convulsions.
- It must not be used as an occlusive dressing, wetpack, or lotion. It must not be used routinely for prophylactic total body bathing.
- It must not be used as a vaginal pack or tampon, or on any mucous membranes.
- pHisoHex must not be used on persons with sensitivity to any of its components. It must not be used on persons who have demonstrated primary light sensitivity to halogenated phenol derivatives because of the possibility of cross-sensitivity to hexachlorophene.
Warnings
There is limited information regarding Hexachlorophene Warnings' in the drug label.
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Hexachlorophene Clinical Trials Experience in the drug label.
Postmarketing Experience
There is limited information regarding Hexachlorophene Postmarketing Experience in the drug label.
Drug Interactions
There is limited information regarding Hexachlorophene Drug Interactions in the drug label.
Use in Specific Populations
Pregnancy
Pregnancy Category (FDA):
There is no FDA guidance on usage of Hexachlorophene in women who are pregnant.
Pregnancy Category (AUS):
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Hexachlorophene in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Hexachlorophene during labor and delivery.
Nursing Mothers
There is no FDA guidance on the use of Hexachlorophene in women who are nursing.
Pediatric Use
There is no FDA guidance on the use of Hexachlorophene in pediatric settings.
Geriatic Use
There is no FDA guidance on the use of Hexachlorophene in geriatric settings.
Gender
There is no FDA guidance on the use of Hexachlorophene with respect to specific gender populations.
Race
There is no FDA guidance on the use of Hexachlorophene with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Hexachlorophene in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Hexachlorophene in patients with hepatic impairment.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Hexachlorophene in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Hexachlorophene in patients who are immunocompromised.
Administration and Monitoring
Administration
There is limited information regarding Hexachlorophene Administration in the drug label.
Monitoring
There is limited information regarding Hexachlorophene Monitoring in the drug label.
IV Compatibility
There is limited information regarding the compatibility of Hexachlorophene and IV administrations.
Overdosage
There is limited information regarding Hexachlorophene overdosage. If you suspect drug poisoning or overdose, please contact the National Poison Help hotline (1-800-222-1222) immediately.
Pharmacology
There is limited information regarding Hexachlorophene Pharmacology in the drug label.
Mechanism of Action
There is limited information regarding Hexachlorophene Mechanism of Action in the drug label.
Structure
There is limited information regarding Hexachlorophene Structure in the drug label.
Pharmacodynamics
There is limited information regarding Hexachlorophene Pharmacodynamics in the drug label.
Pharmacokinetics
There is limited information regarding Hexachlorophene Pharmacokinetics in the drug label.
Nonclinical Toxicology
There is limited information regarding Hexachlorophene Nonclinical Toxicology in the drug label.
Clinical Studies
There is limited information regarding Hexachlorophene Clinical Studies in the drug label.
How Supplied
There is limited information regarding Hexachlorophene How Supplied in the drug label.
Storage
There is limited information regarding Hexachlorophene Storage in the drug label.
Images
Drug Images
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Package and Label Display Panel
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Patient Counseling Information
There is limited information regarding Hexachlorophene Patient Counseling Information in the drug label.
Precautions with Alcohol
Alcohol-Hexachlorophene interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.
Brand Names
There is limited information regarding Hexachlorophene Brand Names in the drug label.
Look-Alike Drug Names
There is limited information regarding Hexachlorophene Look-Alike Drug Names in the drug label.
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.
File:Hexachlorophene.png | |
Clinical data | |
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ATC code | |
Pharmacokinetic data | |
Protein binding | 92% |
Identifiers | |
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CAS Number | |
PubChem CID | |
DrugBank | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C13H6Cl6O2 |
Molar mass | 406.902 g/mol |
Melting point | 164 °C (327.2 °F) |
Hexachlorophene, also known as Nabac, is an antiseptic agent. The compound occurs as a white to light tan crystalline powder which is either odorless or produces a slightly phenolic odor. In medicine, hexachlorophene is very useful as a topical anti-infective, anti-bacterial agent, often used in soaps. It is also used in agriculture as a soil fungicide, plant bactericide, and acaricide.
Two companies had over the counter brands available. One, by The Mennen Company, Morristown, NJ, was known as Baby Magic Bath. Mennen recalled the product and all bottles were taken off retail shelves. Right after the withdrawal, there was an outbreak of Staphylococcus infections in hospitals across the USA.[citation needed]
During the 1960s, a commercial preparation of the drug, pHisoHex, was available over the counter. pHisoHex was widely used as a very effective antibacterial skin cleanser in the treatment of acne. A related product, pHisoAc, was used as a skin mask to dry and peel away acne lesions. Another known as Phiso-Scrub was a hexachlorophene-impregnated sponge for scrubbing; it has since been discontinued.
In 1969 hexachlorophene became suspected of causing cancer. Around 1973 it was withdrawn from over-the-counter sales as a treatment for acne and became a prescription drug. It was later determined not to cause cancer. Nevertheless, hexachlorophene soap is not available over the counter today, because once a product has been withdrawn by the FDA it is virtually impossible for it to be reinstated, even after invalidation of the reasons for its removal. The MSDS still lists this compound as an experimental teratogen.
Possibly because of the previous questions concerning its effects, most dermatologists today do not prescribe it for acne treatment.
Several substitute products (including triclosan) were developed, but none had the germ-killing capability of hexachlorophene.
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