Label: MOISTURIZING SKIN RELIEF- dimethicone 1.2% lotion
- NDC Code(s): 0363-1571-44
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 28, 2024
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- claims
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Inactive ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- Adverse reactions
- principal display panel
-
INGREDIENTS AND APPEARANCE
MOISTURIZING SKIN RELIEF
dimethicone 1.2% lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-1571 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) CETYL ALCOHOL (UNII: 936JST6JCN) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) OATMEAL (UNII: 8PI54V663Y) BENZYL ALCOHOL (UNII: LKG8494WBH) OAT KERNEL OIL (UNII: 3UVP41R77R) STEARETH-20 (UNII: L0Q8IK9E08) SODIUM CHLORIDE (UNII: 451W47IQ8X) SHEA BUTTER (UNII: K49155WL9Y) OAT (UNII: Z6J799EAJK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-1571-44 532 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/17/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 08/17/2020 Labeler - Walgreens (008965063) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(0363-1571)