Active Ingredient
Aluminum Chlorohydrate: 10%
Gerigentle Aloe Dry Anti Perspirant Deodorant Roll On
FDA Label NDC 77573-014
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jiangsu Aimeili Cosmetic Co., Ltd. for the product Gerigentle Aloe Dry Anti Perspirant Deodorant Roll On (NDC 77573-014). 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, otc - purpose, indications & usage, warnings, otc - ask doctor, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose: Anti perspirant
Indications & Usage
Uses Reduces underarm wetness
Warnings
For external use only
Otc - Ask Doctor
Do not use on broken skin. Ask a doctor before use if you have kidney disease
Otc - Stop Use
Stop use if rash or irritation develops
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. Use only as directed.
Directions
Apply to underarm only. Use daily for best results.
Inactive Ingredient
Water, Sorbitol, Hydroxypropyl methylcellulose, Polysorbate 20, Diazolidinyl urea, Fragrance, Triethanolamine
Package Label.Principal Display Panel
Image Description (Gerogental)
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