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Xerac ac - Prescription Drug Labeling

Product NDC Code 0096-0709
Drug Name

Xerac ac

Type Generic
Active Ingredients
Aluminum chloride .0625 g/g
Dosage Form LIQUID
RxCUI drug identifier 197324
Application Number part350
Labeler Name Person and Covey
Package NDC Code Description
0096-0709-35 29.09 g in 1 package (0096-0709-35)
0096-0709-60 49.86 g in 1 package (0096-0709-60)

Active ingredient

A list of the active, medicinal ingredients in the drug product.
OTC - ACTIVE INGREDIENT SECTION Aluminum Chloride Hexahydrate

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
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.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Indicatins and Usage Section For patients suffering from hyperhidrosis, or patients whose jobs or sports activities cause excessive sweating that exacerbates other skin problems.


Information about the drug product’s indications for use.
OTC - PURPOSE SECTION For topical application as an antiperspirant (anhidrotic).

Spl product data elements

Usually a list of ingredients in a drug product.

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Principal Display Panel Xerac AC 35cc Xerac AC 60cc

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION Yes. If swallowed, get medical help or contact a Poison Control Center right away.


Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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.

Disclaimer: Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API