Otc - Active Ingredient
Active Ingredient...........
Aluminum Zirconium Tetrachlorhydrex-Gly........18.0%
Amazing Grace Antiperspirant And Deodorant
FDA Label NDC 53135-825
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Raani Corporation for the product Amazing Grace Antiperspirant And Deodorant (NDC 53135-825). 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 - ask doctor, otc - keep out of reach of children, inactive ingredient, otc - do not use, otc - stop use, 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 - Purpose
Use: Reduces underarm perspiration.
Otc - Ask Doctor
Ask 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.
Inactive Ingredient
cyclopentasiloxane, stearyl alchol, ppg-14 butyl ether, aluminum starch octenyl succinate, hydrogenated castor oil, dimethicone, talc, silica, corn starch, fragrance, squalane, tocopheryl acetate, allantoin, benzyl alcohol, bht.
Otc - Do Not Use
Do not use on broken skin.
Otc - Stop Use
Stop use if rash or irritation occurs.
Package Label.Principal Display Panel
Box Artwork (Agracedeodorantbox)
* Please review the disclaimer below.
