Xerac AC by Person and Covey XERAC AC liquid

Xerac AC by

Drug Labeling and Warnings

Xerac AC by is a Otc medication manufactured, distributed, or labeled by Person and Covey. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

OTC - PURPOSE SECTION

For topical application as an antiperspirant (anhidrotic).

DOSAGE & ADMINISTRATION SECTION

Xerac AC when applied to the underarms, should be applied to absolutely dry skin. Only apply Xerac AC before bedtime, since medication should be kept on the skin for 6-8 hours. To reduce irritation, let the alcohol evaporate, leaving a thin film of antiperspirant on the skin. Wear a T-shirt, while sleeping to prevent medication from being rubbed off on the bed linens. Do not apply Xerac AC to broken, irritated or recently shaved skin. Wash the treated area next morning with soap and water. Do not apply other deodorants or antiperspirants while using Xerac AC.

WARNINGS SECTION

For external use only. Avoid contact with eyes. If contact occurs, wash eyes thoroughly with water. If irritation or sensitization occurs, discontinue use or contact a physician. Xerac AC may be harmful to cotton fibers and certain metals.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Yes. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chloride Hexahydrate

INACTIVE INGREDIENT SECTION

Anhydrous ethanol

Indicatins and Usage Section

For patients suffering from hyperhidrosis, or patients whose jobs or sports activities cause excessive sweating that exacerbates other skin problems.

Principal Display Panel

INGREDIENTS AND APPEARANCE

XERAC AC 
xerac ac liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0096-0709
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B)	ALUMINUM CHLORIDE	0.0625 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0096-0709-60	49.86 g in 1 PACKAGE; Type 0: Not a Combination Product	06/01/1996
2	NDC: 0096-0709-35	29.09 g in 1 PACKAGE; Type 0: Not a Combination Product	06/01/1996

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	06/01/1996

Labeler - Person and Covey (008482473)

Establishment
Name	Address	ID/FEI	Business Operations
Person and Covey		008482473	manufacture(0096-0709)