Label: OIL FREE DAILY FACE EQB- salicylic acid 2% liquid
- NDC Code(s): 79903-208-07
- Packager: Walmart
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated August 23, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingreient Purpose
- PURPOSE
- Use
- Warnings For external use only
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When using this product
avoid contact with the eyes. If product gets into the eyes rinse thoroughly wh 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.limit use to the face and neck
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
wet face
dispense product into hands and massage gently onto face and neck, avoiding the delicate eye area
cover the entire affected area with a thin layer and rinse thoroughly with warm water one to three times daily
because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
if bothersome dryness or peeling occurs, reduce application to once a day or every other day - Other information
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Inactive ingredients
aloe barbadensis leaf juice, fragrance, glycerin, lauric acid, maltodextrin, menthol,
myristic acid, palmitic acid, phenoxyethanol, pentasodium pentetate, polyquaternium-10,
potassium hydroxide, sodium lauroyl sarcosinate, stearic acid, tetrasodium EDTA,
tetrasodium etidronate, triethylene glycol, water. - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
OIL FREE DAILY FACE EQB
salicylic acid 2% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-208 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) PALMITIC ACID (UNII: 2V16EO95H1) MENTHOL (UNII: L7T10EIP3A) POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK) LAURIC ACID (UNII: 1160N9NU9U) ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) EDETATE SODIUM (UNII: MP1J8420LU) PENTASODIUM PENTETATE (UNII: 961TOZ5L7T) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) STEARIC ACID (UNII: 4ELV7Z65AP) ALOE (UNII: V5VD430YW9) MALTODEXTRIN (UNII: 7CVR7L4A2D) GLYCERIN (UNII: PDC6A3C0OX) MYRISTIC ACID (UNII: 0I3V7S25AW) TRIETHYLENE GLYCOL (UNII: 3P5SU53360) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-208-07 184 mL in 1 TUBE; Type 0: Not a Combination Product 08/23/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M006 08/23/2023 Labeler - Walmart (051957769) Registrant - Bridgeview Investments LLC (035014854) Establishment Name Address ID/FEI Business Operations Dimensional Merchandising Inc 076693183 manufacture(79903-208)
