Label: DOVE- manuka honey and retinol smoothing 48h antiperspirant deodorant stick
- NDC Code(s): 64942-2149-1
- Packager: Conopco Inc. d/b/a/ Unilever
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 21, 2024
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- SHEA MOISTURE MANUKA HONEY & RETINOL 48H ANTIPERSPIRANT DEODORANT - aluminum sesquichlorohydrate stick
- Drug Facts
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Directions
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Inactive ingredients
Water (Aqua), C12-15 Alkyl Benzoate, Cyclopentasiloxane, Synthetic Wax, Glycerin, Calcium Chloride, Cetyl PEG/PPG-10/1 Dimethicone, Glycine, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, Butyrospermum Parkii (Shea) Butter, Honey, Retinol, Benzyl Alcohol, Benzyl Cinnamate, Benzyl Salicylate, Citronellol, Coumarin, Farnesol, Hexyl Cinnamal, Limonene, Linalool.
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INGREDIENTS AND APPEARANCE
DOVE
manuka honey and retinol smoothing 48h antiperspirant deodorant stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-2149 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V) ALUMINUM SESQUICHLOROHYDRATE 12.2 g in 100 g Inactive Ingredients Ingredient Name Strength LINALOOL, (+/-)- (UNII: D81QY6I88E) SUNFLOWER OIL (UNII: 3W1JG795YI) BENZYL CINNAMATE (UNII: V67O3RO97U) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) LIMONENE, (+)- (UNII: GFD7C86Q1W) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CALCIUM CHLORIDE (UNII: M4I0D6VV5M) WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099) GLYCERIN (UNII: PDC6A3C0OX) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) (UNII: 8INO2K35FA) GLYCINE (UNII: TE7660XO1C) RETINOL (UNII: G2SH0XKK91) SHEA BUTTER (UNII: K49155WL9Y) BENZYL ALCOHOL (UNII: LKG8494WBH) HONEY (UNII: Y9H1V576FH) COUMARIN (UNII: A4VZ22K1WT) BENZYL SALICYLATE (UNII: WAO5MNK9TU) FARNESOL (UNII: EB41QIU6JL) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-2149-1 74 g in 1 CONTAINER; Type 0: Not a Combination Product 10/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M019 10/01/2023 Labeler - Conopco Inc. d/b/a/ Unilever (001375088) Registrant - Conopco Inc. d/b/a/ Unilever (001375088) Establishment Name Address ID/FEI Business Operations KDC/ONE Development Corporation, Inc 204006464 manufacture(64942-2149)