Label: DOVE- moisturizing hand sanitizer wipes shea butter and warm vanilla scent gel
- NDC Code(s): 64942-2030-1, 64942-2030-2
- Packager: Conopco Inc. d/b/a/ Unilever
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 May 11, 2022
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- Official Label (Printer Friendly)
- DOVE MOISTURIZING HAND SANITIZER WIPES SHEA BUTTER & WARM VANILLA SCENT - ethyl alcohol cloth
- Drug Facts
- Purpose
- Uses
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Warnings
For external use only
Flammable. Keep away from fire or flameDo not store in car
Do not use in children less than 12 months of age
Do not use on open skin wounds
When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask doctor if irritation or redness develop - KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Questions?
- Packaging
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INGREDIENTS AND APPEARANCE
DOVE
moisturizing hand sanitizer wipes shea butter and warm vanilla scent gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-2030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 760 mg in 1 mL Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP) COUMARIN (UNII: A4VZ22K1WT) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) LIMONENE, (+)- (UNII: GFD7C86Q1W) NIACINAMIDE (UNII: 25X51I8RD4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) EDETATE SODIUM (UNII: MP1J8420LU) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) LINALOOL, (+/-)- (UNII: D81QY6I88E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-2030-2 20 in 1 POUCH 07/21/2020 1 NDC:64942-2030-1 8.57 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 07/21/2020 Labeler - Conopco Inc. d/b/a/ Unilever (001375088)