DOVE CLINICAL PROTECTION POWDER SOFT ANTIPERSPIRANT AND DEODORANT- aluminum zirconium tetrachlorohydrex gly stick

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]

ACTIVE INGREDIENT

Active Ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (20%)

PURPOSE

Purpose
anti-perspirant

INDICATIONS & USAGE

Uses

reduces underarm wetness
extra effective

WARNINGS

Warnings
For external use only

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash or irritation occurs

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

DOSAGE & ADMINISTRATION

Directions

apply to underarms only
before bed, apply two clicks of product to each underarm

INACTIVE INGREDIENT

Inactive ingredients
Cyclopentasiloxane, Dimethicone, Paraffin, Microcrystalline Wax, Silica, Fragrance (Parfum), Helianthus Annuus  (Sunflower) Seed Oil, Dimethicone Crosspolymer, BHT.

QUESTIONS

Questions?  Call toll-free 1-800-761-3683

1.7 oz PDP

1.7 oz carton

INGREDIENTS AND APPEARANCE

DOVE  CLINICAL PROTECTION POWDER SOFT ANTIPERSPIRANT AND DEODORANT
aluminum zirconium tetrachlorohydrex gly stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1393
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Aluminum Zirconium Tetrachlorohydrex GLY (UNII: 8O386558JE) (Aluminum Zirconium Tetrachlorohydrex GLY - UNII:8O386558JE)	Aluminum Zirconium Tetrachlorohydrex GLY	20 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SUNFLOWER OIL (UNII: 3W1JG795YI)
PARAFFIN (UNII: I9O0E3H2ZE)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1393-2	1 in 1 CARTON
1	NDC: 64942-1393-1	48 g in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	12/15/2015

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