CLARISSE ANTIPERSPIRANT DEODORANT DAILY PROTECTION- aluminum chlorohydrate stick

CLARISSE Antiperspirant Deodorant by

Drug Labeling and Warnings

CLARISSE Antiperspirant Deodorant by is a Otc medication manufactured, distributed, or labeled by Delta Brands Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Aluminum chlorohydrate 20%

Purpose

Antiperspirant

Use

reduces underarm wetness and perspiration

Warnings

For external use only

Do not use

on broken or irritated skin.

Ask a doctor before use ​

if you have kidney disease

Stop use and ask a doctor

if irritation or rash develops

Keep out of reach of children

If swallowed, seek medical help or contact a Poison Control Center immediately.

Directions

remove cap, turn dial to raise product, apply evenly to underarms only, replace cap after use.

Inactive ingredients

mineral oil, stearic acid, stearyl alcohol, talc, zinc palmitate, cyclopentasiloxane, hydrogenated castor oil, fragrance, silica, PPG-14 butyl ether, PEG-8 distearate, butylated hydroxytoluene

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLARISSE ANTIPERSPIRANT DEODORANT  DAILY PROTECTION
aluminum chlorohydrate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-700
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	20 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
STEARIC ACID (UNII: 4ELV7Z65AP)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
TALC (UNII: 7SEV7J4R1U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ZINC PALMITATE (UNII: Q7407964JA)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
MINERAL OIL (UNII: T5L8T28FGP)
PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-700-57	57 g in 1 APPLICATOR; Type 0: Not a Combination Product	10/17/2016
2	NDC: 20276-700-64	64 g in 1 APPLICATOR; Type 0: Not a Combination Product	10/17/2016
3	NDC: 20276-700-71	71 g in 1 APPLICATOR; Type 0: Not a Combination Product	10/17/2016
4	NDC: 20276-700-51	51 g in 1 APPLICATOR; Type 0: Not a Combination Product	04/12/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	10/17/2016

Labeler - Delta Brands Inc (102672008)