XERAC AC- xerac ac liquid 
Person and Covey

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Xerac AC

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 35ccXerac AC 60cc

XERAC AC 
xerac ac liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0096-0709
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE0.0625 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0096-0709-6049.86 g in 1 PACKAGE; Type 0: Not a Combination Product06/01/1996
2NDC:0096-0709-3529.09 g in 1 PACKAGE; Type 0: Not a Combination Product06/01/1996
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01906/01/1996
Labeler - Person and Covey (008482473)
Establishment
NameAddressID/FEIBusiness Operations
Person and Covey008482473manufacture(0096-0709)

Revised: 1/2024
Document Id: 0cf901e1-366d-5d21-e063-6394a90af9af
Set id: 59e37deb-01da-465f-b806-ff1a76255e71
Version: 12
Effective Time: 20240101
 
Person and Covey