Aluminum Chlorohydrate
FDA Label NDC 47993-331

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Jiangbei Ocean Star Trading Co.,ltd for the product Aluminum Chlorohydrate (NDC 47993-331). 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 - stop use, 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.

Label Section Quick Index

Otc - Active Ingredient

Active ingredients
Aluminum Chlorohydrate, 10%

Otc - Purpose

Antiperspirant

Indications & Usage

Uses：

Helps lessen underarm perspiration.

Warnings

Warnings:

Do not use on broken skin.

Otc - Stop Use

Stop use if rash or irritation occurs. Ask a doctor before use 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 a Poison Control Center right away.

Dosage & Administration

Directions:

Apply thin layer to underarm.

Inactive Ingredient

Inactive Ingredients:

Aqua, Dipropylene Glycol, Peg-40 Hydrogenated Castor Oil, Polysorbate 20, Parfum, Hydroxyethylcellulose, Phenoxyethanol, Menthol, Disodium Edta.

Package Label.Principal Display Panel

Image Of Hand Sanitizer 56.7g (56.7g)

Image Of Hand Sanitizer 56.7g (56.7g)

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