BABY DOVE- 8h moisturization hand sanitizer fragrance free gel

Baby Dove by

Drug Labeling and Warnings

Baby 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]

BABY DOVE 8H MOISTURIZATION HAND SANITIZER FRAGRANCE FREE - Ethyl Alcohol gel

Baby Dove 8h Moisturization Hand Sanitizer

Drug Facts

Active ingredient

Alcohol (61%)

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria on the skin

Warnings

For external use only
Flammable. Keep away from fire or flame, Do not store in car.
Avoid contact with eyes, in case of contact, rinse eyes thoroughly with water immediately.

If irritation develps, discontinue use and consult a doctor.

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

Not recommended for use on infants (younger than 12 months).
Children under 6 years of age should be supervised when using this product.
Place enough product in your palm to thoroughly cover your hands and rub hands togeter briskly until dry.
for babies 1 year*, rub their hands in yours and do not let them touch their eyes right after rubbing
Allow to dry without wiping or rinsing

Other information

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

Inactive ingredients

Water (Aqua), Glycerin, Butylene Glycol, Dimethicone, Glycine Soja (Soybean) Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Echium Plantagineum Seed Oil, Aminomethyl Propanol, Hydrogenated Lecithin, Tocopherol, Xanthan Gum, Stearic Acid, Citric Acid, Benzyl Alcohol

Questions or Comments?

Call 1-800-761-DOVE(3683) or visit us at www.babydove.com

Packaging

INGREDIENTS AND APPEARANCE

BABY DOVE 
8h moisturization hand sanitizer fragrance free gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-2036
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	610 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
TOCOPHEROL (UNII: R0ZB2556P8)
SOYBEAN OIL (UNII: 241ATL177A)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
XANTHAN GUM (UNII: TTV12P4NEE)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)
STEARIC ACID (UNII: 4ELV7Z65AP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-2036-1	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/15/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	07/15/2022

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