Pure Grace Antiperspirant And Deodorant
FDA Label NDC 53135-925

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 Pure Grace Antiperspirant And Deodorant (NDC 53135-925). 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, inactive ingredient, otc - purpose, otc - ask doctor, otc - keep out of reach of children, 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 - Active Ingredient

Active Ingredient.............

Aluminum Zirconium Tetrachlorhydrex-gly.......18.0%


Inactive Ingredient

CYCLOPTENTASILOXANE      36.15%

STEARYL ALCOHOL              20.0%

PPG-14 BUTYL ETHER          10.0%

ALUMINUM STARCH OCTENYL SUCCINATE     3.0%

HYDROGENATED CASTOR OIL     3.0%

DIMETHICONE    2.10%

TALC   2.0%

SILICA     1.0%

CORN STARCH    1.0%

FRAGRANCE     1.0%

SQUALANE     0.05%

TOCOPHERYL ACETATE   0.04%

ALLANTOIN     0.0005%

BENZYL ALCOHOL    0.0003%

BHT     0.0002%

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.

Otc - Do Not Use

DO NOT USE ON BROKEN SKIN.

Otc - Stop Use

Enter section text here

Package Label.Principal Display Panel

Pgracedeodorantbox.jpg (Pgracedeodorantbox)

Pgracedeodorantbox.jpg (Pgracedeodorantbox)

* Please review the disclaimer below.