Label: H.E.B. OIL FREE DAILY ACNE SCRUB- salicylic acid cream
- NDC Code(s): 37808-342-73
- Packager: H.E.B
- 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 May 16, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
- Sunburn Alert:
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Directions
- cover the entire affected area with a think layer and rinse thoroughly 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
water, cetyl alcohol, PPG-15 stearyl ether, hydrogenated jojoba oil, glycolic acid, glycerin, polysorbate 60, steareth-21, C12-15 alkyl lactate, cetyl lactate, tocopheryl acetate, tetrahexyldecyl ascorbate, butyrospermum parkii (shea butter), cetyl lactate, neopentyl glycol dicaprylate/dicaprate, cocamidopropyl PG-dimonium chloride phosphate, potassium cetyl phosphate, disodium EDTA, xanthan gum, sodium chloride, sodium benzotriazolyl butylphenol sulfonate, sodium hydroxide, agar, corn starch/acrylamide/sodium copolymer, menthol, fragrance, mica, iron oxide, red 30, red 40, yellow 5.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
H.E.B. OIL FREE DAILY ACNE SCRUB
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-342 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) EDETATE DISODIUM (UNII: 7FLD91C86K) CETYL ALCOHOL (UNII: 936JST6JCN) PPG-15 STEARYL ETHER (UNII: 1II18XLS1L) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) GLYCOLIC ACID (UNII: 0WT12SX38S) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 60 (UNII: CAL22UVI4M) STEARETH-21 (UNII: 53J3F32P58) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 40 (UNII: WZB9127XOA) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) SHEA BUTTER (UNII: K49155WL9Y) CETYL LACTATE (UNII: A7EVH2RK4O) NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z) SODIUM HYDROXIDE (UNII: 55X04QC32I) AGAR (UNII: 89T13OHQ2B) MENTHOL (UNII: L7T10EIP3A) MICA (UNII: V8A1AW0880) D&C RED NO. 30 (UNII: 2S42T2808B) FERRIC OXIDE RED (UNII: 1K09F3G675) HYDROGENATED JOJOBA OIL (UNII: 7F674YQ5SO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-342-73 125 mL in 1 TUBE; Type 0: Not a Combination Product 02/26/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 02/26/2021 Labeler - H.E.B (007924756)