Label: 5% BENZOYL PEROXIDE FOLLICULITIS CREAM cream
- NDC Code(s): 84558-026-01
- Packager: GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 16, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
-
WHEN USING
.avoid unnecessary sun exposure and use a sunscreen.
.avoid contact with the eyes, lips, and mouth.
.avoid contact with hair and dyed fabrics, which may be bleached by this product.
.skin irritation may occur, characterized by redness, burning, itching,
peeling, or swelling. Reduce frequency of use if irritation occurs. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
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Inactive ingredients
Water, Glycerin, C12-15 Alkyl Benzoate, Propylene Glycol, Glyceryl
Stearate, Cetearyl Alcohol, Squalane, Aloe Barbadensis Leaf Juice,
Dimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate
Copolymer, Phenoxyethanol, Panthenol, PEG-100 Stearate,
Polysorbate 80, Magnesium Aluminum Silicate, Ceramide NP,Sodium
Hydroxide, Allantoin, Scutellaria Baicalensis Root Extract, Forsythia
Suspensa Fruit Extract, Portulaca Oleracea Extract, Magnolia Officinalis
Bark Extract,Calendula Officinalis Flower Extract, Melaleuca Alternifolia
(Tea Tree) Leaf Oil, Menthy| Lactate, Ethylhexylglycerin, Disodium EDTA - Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
5% BENZOYL PEROXIDE FOLLICULITIS CREAM
5% benzoyl peroxide folliculitis cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84558-026 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 5 g in 100 g Inactive Ingredients Ingredient Name Strength CERAMIDE NP (UNII: 4370DF050B) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) AQUA (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERYL STEARATE (UNII: 230OU9XXE4) CETEARYL ALCOHOL (UNII: 2DMT128M1S) SQUALANE (UNII: GW89575KF9) ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB) DIMETHICONE (UNII: 92RU3N3Y1O) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) DEXPANTHENOL (UNII: 1O6C93RI7Z) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALLANTOIN (UNII: 344S277G0Z) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G) MAGNESIUM ALUMINOMETASILICATE (UNII: 9T3UU8T0QK) FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5) PURSLANE (UNII: M6S840WXG5) MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974) PEG-100 STEARATE (UNII: YD01N1999R) SODIUM HYDROXIDE (UNII: 55X04QC32I) MENTHYL LACTATE (UNII: 2BF9E65L7I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84558-026-01 100 g in 1 BOTTLE; Type 0: Not a Combination Product 07/17/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 07/17/2026 Labeler - GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd (545488483) Establishment Name Address ID/FEI Business Operations GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd 545488483 manufacture(84558-026)

