Label: AVEENO CLEAR COMPLEXION DAILY MOISTURIZER- salicylic acid lotion
- NDC Code(s): 69968-0372-4
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
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 January 6, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
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Directions
- Clean the skin thoroughly before applying this product
- Cover the entire affected area with a thin layer 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, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Dimethicone, Methyl Gluceth-20, PPG-10 Cetyl Ether, Bis-Phenylpropyl Dimethicone, Arachidyl Alcohol, Behenyl Alcohol, Glycine Soja (Soybean) Seed Extract, Glycerin, Isoceteth-20, Polyacrylamide, Cetearyl Glucoside, Arachidyl Glucoside, C13-14 Isoparaffin, Ethylene/Acrylic Acid Copolymer, Fragrance, Laureth-7, Disodium EDTA, BHT, Sodium Hydroxide, Citric Acid
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
AVEENO CLEAR COMPLEXION DAILY MOISTURIZER
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0372 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) BIS-PHENYLPROPYL DIMETHICONE (15 CST) (UNII: 4836494CFT) PPG-10 CETYL ETHER (UNII: Q056X4917J) METHYL GLUCETH-20 (UNII: J3QD0LD11P) DIMETHICONE (UNII: 92RU3N3Y1O) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) SOYBEAN (UNII: L7HT8F1ZOD) ISOCETETH-20 (UNII: O020065R7Z) DOCOSANOL (UNII: 9G1OE216XY) GLYCERIN (UNII: PDC6A3C0OX) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I) LAURETH-7 (UNII: Z95S6G8201) SODIUM HYDROXIDE (UNII: 55X04QC32I) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0372-4 1 in 1 CARTON 01/01/2004 1 118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 01/01/2004 Labeler - Johnson & Johnson Consumer Inc. (118772437)