Roll On Anti-perspirant Deodorant Solution
FDA Label NDC 51870-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Keefe Group for the product Roll On Anti-perspirant Deodorant (NDC 51870-001). 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 other, active ingredient, purpose, use, warnings, otc - keep out of reach of children, otc - do not use, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Distributed by:
Olivette Products, L.L.C., Bridgeton, MO 63044

Active Ingredient

Aluminum Chlorohydrate, 14% – Anhydrous Basis

Purpose

Antiperspirant

Use

Reduces underarm wetness.

Warnings

For external use only.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Otc - Do Not Use

Do not use on broken skin.

Otc - Stop Use

Stop use if rash or irritation occurs.

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

Directions

Apply to underarms only.

Inactive Ingredients

Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Fragrance, Tetrasodium EDTA

Principal Display Panel - 88 Ml Bottle Label

FORCE

POWER UP
ANTI-PERSPIRANT
& DEODORANT ROLL-ON

3 fl oz/88 ml

Principal Display Panel (88 ml Bottle Label)

Principal Display Panel (88 ml Bottle Label)

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