Label: DAILY MOISTURIZING- dimethicone lotion
- NDC Code(s): 49035-619-40, 49035-619-44
- Packager: Wal-Mart Stores, Inc
- 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 February 22, 2022
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- Claims
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- When using
- Stop use
- Keep out of reach of children
- Directions
- Inactive ingredients
- disclaimer
- Adverse Reactions
- principal display panel
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INGREDIENTS AND APPEARANCE
DAILY MOISTURIZING
dimethicone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-619 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 13.13 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) OATMEAL (UNII: 8PI54V663Y) BENZYL ALCOHOL (UNII: LKG8494WBH) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-619-40 354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/22/2010 2 NDC:49035-619-44 532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/22/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 02/22/2010 Labeler - Wal-Mart Stores, Inc (051957769) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(49035-619) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(49035-619)