Active Ingredient

Salicylic Acid 2%

Purpose

Acne Medication

Uses

For the treatment of acne.

Warnings

For External use only.

When using this product

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

Keep out of reach of children.

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

Directions

Wet face.
dispense product into hands, lather and massage gently onto face and neck, avoiding the delicate eye area.
Rinse thoroughly with warm water and pat dry.
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.

Inactive Ingredients

Water (Aqua), Hydrated Silica, PPG-15 Stearyl Ether, Stearyl Alcohol, Glycerin, Distearyldimonium Chloride, Microcrystalline Cellulose, Cetyl Alcohol, Steareth-2, Behenyl Alcohol, Fragrance (Parfum), Steareth-21, Silica, Xanthan Gum, Synthetic Wax, Cetyl Betaine, Caprylyl Glycol, 1,2-Hexanediol, Sodium Hydroxide, Disodium EDTA, Sodium Chloride, Microcrystalline Wax, Sodium Lauryl Sulfate, Blue 1 Lake (CI 42090), Blue 1 (CI 42090).

Questions/comments?

1-888-287-1915

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salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79903-317
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
EDETATE DISODIUM (UNII: 7FLD91C86K)
PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
XANTHAN GUM (UNII: TTV12P4NEE)
WATER (UNII: 059QF0KO0R)
SYNTHETIC WAX (540 MW) (UNII: DW2TC44JRY)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
STEARETH-2 (UNII: V56DFE46J5)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
STEARETH-21 (UNII: 53J3F32P58)
CETYL ALCOHOL (UNII: 936JST6JCN)
BEHENYL ALCOHOL (UNII: 9G1OE216XY)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CETYL BETAINE (UNII: E945X08YA9)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
BLUE 1 LAKE (UNII: J9EQA3S2JM)
SILICA (UNII: ETJ7Z6XBU4)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:79903-317-68	200 mL in 1 TUBE; Type 0: Not a Combination Product	04/01/2025

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	04/01/2025

Labeler - Walmart INC (051957769)

Registrant - Apollo Health and Beauty Care (201901209)

Name	Address	ID/FEI	Business Operations
Establishment
Apollo Health and Beauty Care		201901209	manufacture(79903-317)

NDC- 79903-317, Acne Control 5 in 1 Exfoliating Wash.