2.25OZ EVERDRY ULTRA DRY ANTIPERSPIRANT- aluminum chlorohydrate gel stick

2.5OZ EverDry Antiperspirant Invisible by

Drug Labeling and Warnings

2.5OZ EverDry Antiperspirant Invisible by is a Otc medication manufactured, distributed, or labeled by American Consumer Products Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Aluminum Chlorohydrate 20%

PURPOSE

Purpose: Antiperspirant

WARNINGS

Warnings:For external use only.

KEEP OUT OF REACH OF CHILDREN

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

INACTIVE INGREDIENT

Ingredients: Mineral Oil, Stearic Acid, Stearyl Alcohol, Zinc, Palmitate, Cyclopentasiloxane, Hydrogenated Castor Oil, Fragrance, Silica, PPG-14 Butyl Ether, PEG-8 Disterate, BHT.

DOSAGE & ADMINISTRATION

Directions: Twist base. Smooth onto dry underarms. Apply to underarms only.

INSTRUCTIONS FOR USE

Use: reduces underarm wetness and perspiration.

STOP USE

Stop use and ask a doctor if irritation or rash develops.

INDICATIONS & USAGE

Do not use on broken or irritated skin.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

2.25OZ EVERDRY ULTRA DRY ANTIPERSPIRANT 
aluminum chlorohydrate gel stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-018
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)
MINERAL OIL (UNII: T5L8T28FGP)
STEARIC ACID (UNII: 4ELV7Z65AP)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
LAURYL PALMITATE (UNII: X3V3247O54)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
ZINC (UNII: J41CSQ7QDS)
TALC (UNII: 7SEV7J4R1U)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-018-02	63.78 g in 1 TUBE; Type 0: Not a Combination Product	09/17/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	09/17/2019

Labeler - American Consumer Products Corp (081101181)