Gandh Protect Antiperspirant Deodorant Roll On Gel
FDA Label NDC 10056-534

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Access Business Group Llc for the product Gandh Protect Antiperspirant Deodorant Roll On (NDC 10056-534). 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 active ingredient, purpose, uses, warnings, do not use, stop use if, ask doctor before use, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Aluminum Chlorohydrate 25%

Purpose

Antiperspirant

Uses

Reduces underarm wetness.

Warnings

  • For external use only.

Do Not Use

  • on broken skin.

Stop Use If

rash or irritation occurs.

Ask Doctor Before Use

  • if you have kidney disease.

Keep Out Of Reach Of Children.

  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Shake before use. Apply to underarms only.

Inactive Ingredients:

Water, PPG-3 Myristyl Ether, Steareth-2, Steareth-20, Sodium Benzoate, Glycerin, Fragrance, Glycine, Allantoin, Caprylic/Capric Triglyceride, Lauric Acid, Propylene Glycol, Butylene Glycol, Bisabolol, Lecithin, Centella Asiatica Extract, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Camellia Sinensis Leaf Extract, Myristic Acid, Phenoxyethanol, Rosmarinus Officinalis (Rosemary) Leaf Extract, Ceramide NP, Beta-Sitosterol, Chlorphenesin, Zingiber Officinale (Ginger) Root Extract, Tocopherol, Geraniol, Limonene, Linalool

Package Labeling:

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