DOVE- hand sanitizer wipes shea butter and warm vanilla scent cloth

Dove by

Drug Labeling and Warnings

Dove by is a Otc medication manufactured, distributed, or labeled by Conopco Inc. d/b/a/ Unilever. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOVE MOISTURIZING HAND SANITIZER WIPES SHEA BUTTER & WARM VANILLA SCENT - ethyl alcohol cloth

Dove Nourishing Hand Sanitizer Shea Butter & Warm Vanilla 8h Moisturization

Drug Facts

Active ingredient

Ethyl Alcohol 76%

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

For external use only
Flammable. Keep away from fire or flame

Do 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

Keep out of reach of children except under adult supervision.

If swallowed, get medical help or contact a poison control Center right away.

Directions

Wet hands thoroughly with product and rub lightly until dry.

Other information

Avoid excessive heat. Store below 105˚F (40˚C).
May discolor fabrics or surfaces.

Inactive ingredients

Water (Aqua), Glycerin, Butylene Glycol, Fragrance (Parfum), Niacinamide, Tocopheryl Acetate, Stearic Acid, Tetrasodium EDTA, Coumarin, Hexyl Cinnamal, Limonene, Linalool.

Questions?

1-800-761-3683

Packaging

INGREDIENTS AND APPEARANCE

DOVE 
hand sanitizer wipes shea butter and warm vanilla scent cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-2041
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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
NIACINAMIDE (UNII: 25X51I8RD4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-2041-2	20 in 1 POUCH	05/20/2022
1	NDC: 64942-2041-1	8.57 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 64942-2041-4	40 in 1 POUCH	05/20/2022
2	NDC: 64942-2041-3	8.57 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	05/20/2022

Labeler - Conopco Inc. d/b/a/ Unilever (001375088)