BABY DOVE- eczema care soothing cream cream

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]

Description

BABY DOVE ECZEMA CARE SOOTHING CREAM - (colloidal oatmeal) cream

Drug Facts

Active ingredient
Colloidal Oatmeal (1%)

Purpose

Skin Protectant

Uses

temporarily protects and helps relieve minor skin irritation and itching due to:

• eczema

Warnings

For external use only
When using this product do not get into eyes.r.
Stop use and ask a doctor if

• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply as needed

Other Information

Do not use if tamper evident seal is missing or broken.

Inactive ingredients

Water (Eau), Glycerin, Dimethicone, Butyrospermum Parkii (Shea) Butter, Copernicia Cerifera (Carnauba) Wax, Isopropyl Myristate, Cetearyl Alcohol, Glyceryl Hydroxystearate, Dimethicone Crosspolymer, Hydroxystearic Acid, Caprylyl Glycol, Cetearyl Glucoside, Sodium Cetearyl Sulfate, Cetyl Palmitate, Sodium Benzoate, Phenoxyethanol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Stearic Acid, Tetrasodium EDTA.

Questions or comments?

1-800-761-3683

Packaging

INGREDIENTS AND APPEARANCE

BABY DOVE 
eczema care soothing cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1873
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y)	OATMEAL	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
STEARIC ACID (UNII: 4ELV7Z65AP)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
SHEA BUTTER (UNII: K49155WL9Y)
DIMETHICONE (UNII: 92RU3N3Y1O)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
CARNAUBA WAX (UNII: R12CBM0EIZ)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERYL HYDROXYSTEARATE (UNII: UJ6CAW9YNV)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
12-HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
CETYL PALMITATE (UNII: 5ZA2S6B08X)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE SODIUM (UNII: MP1J8420LU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1873-1	144 mL in 1 TUBE; Type 0: Not a Combination Product	03/05/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	03/05/2021

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