Xerac AC: Package Insert and Label Information

XERAC AC- aluminum chloride liquid
Person and Covey

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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

Xerac AC 35cc
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Xerac AC 60cc
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XERAC AC
xerac ac liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0096-0709
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALUMINUM CHLORIDE (ALUMINUM CATION) ALUMINUM CHLORIDE 0.0625 g in 1 g
Inactive Ingredients
Ingredient Name Strength
ALCOHOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0096-0709-60 49.86 g in 1 PACKAGE None
2 NDC:0096-0709-35 29.09 g in 1 PACKAGE None
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 Operations
Person and Covey 008482473 manufacture (0096-0709)

Revised: 01/2020 Person and Covey

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