Antiperspirant
FDA Label NDC 22431-641

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Blue Cross Labs for the product Antiperspirant (NDC 22431-641). 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, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredient Purpose

Aluminum Zirconium tetrachlorohydrex Gly 8.6% W/W Antiperspirant

Otc - Purpose

Use reduces underarm perspiration

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.

Indications & Usage

Stop use and ask a doctor if rash or irritation occurs.

Warnings


Warnings
For external use only
Do not use on broken skin

Dosage & Administration

Directions apply to underarms only

Inactive Ingredient

Inactive ingredients

Propylene glycol, fragrance, dibenzylidene sorbitol, diisopropyl sebacate, hydroxypropyl cellulose, PEG/PPG-14/4 dimethicone, tetrasodium EDTA.

Package Label.Principal Display Panel

Maximum Security

Antiperspirant

Regular

Net WT. 2.5 oz (70g)

Image Description (Front)

Image Description (Front)

Image Of Back (Back)

Image Of Back (Back)

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