Label: AVEENO SKIN RELIEF MOISTURIZING FRAGRANCE FREE- dimethicone lotion
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NDC Code(s):
69968-0408-1,
69968-0408-2,
69968-0408-3,
69968-0408-4, view more69968-0408-8
- 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 4, 2023
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- Active Ingredient
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- Inactive Ingredients
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 532 mL Bottle Label
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INGREDIENTS AND APPEARANCE
AVEENO SKIN RELIEF MOISTURIZING FRAGRANCE FREE
dimethicone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0408 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 12 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X) PETROLATUM (UNII: 4T6H12BN9U) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) CETYL ALCOHOL (UNII: 936JST6JCN) OATMEAL (UNII: 8PI54V663Y) BENZYL ALCOHOL (UNII: LKG8494WBH) OAT KERNEL OIL (UNII: 3UVP41R77R) STEARETH-20 (UNII: L0Q8IK9E08) SODIUM CHLORIDE (UNII: 451W47IQ8X) SHEANUT (UNII: 84H6HBP32L) OAT (UNII: Z6J799EAJK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0408-1 29 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2005 2 NDC:69968-0408-8 227 mL in 1 TUBE; Type 0: Not a Combination Product 12/01/2005 06/07/2022 3 NDC:69968-0408-2 354 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2005 4 NDC:69968-0408-3 532 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2005 5 NDC:69968-0408-4 24 in 1 CARTON 12/01/2005 5 29 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 12/01/2005 Labeler - Johnson & Johnson Consumer Inc. (118772437)