Amerfresh Roll-on Antiperspirant Deodorant
FDA Label NDC 51460-4974

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Amercare Products, Inc for the product Amerfresh Roll-on Antiperspirant Deodorant (NDC 51460-4974). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - ask doctor, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

DRUG FACTS

Active Ingredients                              Purpose

Aluminum Chlorohydrate 1%              Antiperspirant

Otc - Purpose

Purpose

Antiperspirant

Indications & Usage

Uses

Reduces underarm wetness

Warnings

WARNINGS  

For external use only

Do not use on broken skin

Stop use if rash or irritation occurs


Otc - Ask Doctor

Ask a doctor before using if you have kidney disease

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Dosage & Administration

DIRECTIONS: apply to underarms only.

Inactive Ingredient

INACTIVE INGREDIENTS:

Fragrance, Glyceryl stearate, magnesium aluminum silicate, peg100 stearate, water

Other

Distributed by:

Amercare Products, Inc.

Seattle, WA 98125

PRODUCT OF CHINA

To report a serious or adverse event

Contact (425) 489-9575

Package Label.Principal Display Panel

AMERFRESH

ROLL-ON ANTIPERSPIRANT DEODORANT

1.5 fl. oz (44ml)


Amerfreshrollon (Rollon)

Amerfreshrollon (Rollon)

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