OTC Medication Information: PHisoderm CLEAN ANTI-BLEMISH FACIAL CLEANSER

PHISODERM CLEAN ANTI-BLEMISH FACIAL CLEANSER- salicylic acid gel
The Mentholatum Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Uses

For the treatment of acne

Warnings

For external use only

When using this product

avoid contact with eyes. If contact occurs, flush thoroughly with water.
skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet face, then gently massage cleanser onto skin
rinse well and pat dry
use twice daily

Inactive ingredients

water, lauramidopropyl betaine, sodium C14-16 olefin sulfonate, lauryl glucoside, aloe barbadensis leaf juice, aminomethyl propanol, butylene glycol, caprylyl/capryl glucoside, carica papaya (papaya) fruit extract, chamomilla recutita (matricaria) flower extract, disodium EDTA, fragrance, glycerin, hydroxyphenyl propamidobenzoic acid, hydroxypropyltrimonium hyaluronate, pentylene glycol, potassium sorbate, sodium benzoate, sodium chloride, tocopheryl acetate [vitamin E]

Questions?

1-877-636-2677 MON-FRI 9 AM to 5 PM (EST)

Principal Display Panel

pHisoderm CLEAN ANTI-BLEMISH FACIAL CLEANSER
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Drug Facts
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PHISODERM CLEAN ANTI-BLEMISH FACIAL CLEANSER
salicylic acid gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-1235
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID 20 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
LAURAMIDOPROPYL BETAINE
SODIUM C14-16 OLEFIN SULFONATE
LAURYL GLUCOSIDE
ALOE VERA LEAF
AMINOMETHYLPROPANOL
BUTYLENE GLYCOL
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE
PAPAYA
CHAMOMILE
EDETATE DISODIUM
GLYCERIN
HYDROXYPHENYL PROPAMIDOBENZOIC ACID
DIHYDROXYPROPYLTRIMONIUM
PENTYLENE GLYCOL
POTASSIUM SORBATE
SODIUM BENZOATE
SODIUM CHLORIDE
.ALPHA.-TOCOPHEROL ACETATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:10742-1235-1 177 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333D 07/02/2021
Labeler — The Mentholatum Company (002105757)

Revised: 07/2021 The Mentholatum Company

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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