NDC 53135-925 Pure Grace Antiperspirant And Deodorant

NDC Product Code 53135-925

NDC 53135-925-02

Package Description: 1 TUBE in 1 BOX > 85 g in 1 TUBE (53135-925-01)

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Pure Grace Antiperspirant And Deodorant with NDC 53135-925 is a product labeled by Raani Corporation. The generic name of Pure Grace Antiperspirant And Deodorant is . The product's dosage form is and is administered via form.

Labeler Name: Raani Corporation

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • TALC (UNII: 7SEV7J4R1U)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • SQUALANE (UNII: GW89575KF9)
  • .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
  • ALLANTOIN (UNII: 344S277G0Z)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • PPG-14 BUTYL ETHER (UNII: R199TJT95T)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Raani Corporation
Labeler Code: 53135
Start Marketing Date: 02-28-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Pure Grace Antiperspirant And Deodorant Product Label Images

Pure Grace Antiperspirant And Deodorant Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling 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

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