Label: DAILY MOISTURIZING- dimethicone lotion
- NDC Code(s): 11822-0619-1, 11822-0619-2, 11822-0619-3
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 19, 2024
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- Official Label (Printer Friendly)
- active ingredient
- Purpose
- Uses
- Warnings
- Do not use on
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Inactive ingredients
- Disclaimer
- Adverse Reaction
- Principal display panel
- Principal display panel
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INGREDIENTS AND APPEARANCE
DAILY MOISTURIZING
dimethicone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0619 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 13 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) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0619-1 354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/23/2012 2 NDC:11822-0619-2 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/23/2012 3 NDC:11822-0619-3 225 mL in 1 TUBE; Type 0: Not a Combination Product 06/19/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 04/23/2012 Labeler - Rite Aid Corporation (014578892) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(11822-0619)