NDC 15197-007 Bodyglide Anti Chafe Balm

NDC Product Code 15197-007

NDC 15197-007-07

Package Description: 2 g in 1 TUBE

NDC 15197-007-14

Package Description: 1 TUBE in 1 PACKAGE > 36.9 g in 1 TUBE (15197-007-13)

NDC 15197-007-26

Package Description: 1 TUBE in 1 PACKAGE > 70 g in 1 TUBE (15197-007-25)

NDC 15197-007-46

Package Description: 1 TUBE in 1 PACKAGE > 12.8 g in 1 TUBE (15197-007-45)

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

NDC Product Information

Bodyglide Anti Chafe Balm with NDC 15197-007 is product labeled by W Sternoff Llc. The product's dosage form is and is administered via form.

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.

  • ALOE (UNII: V5VD430YW9)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)

Product Labeler Information

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

Labeler Name: W Sternoff Llc
Labeler Code: 15197
Start Marketing Date: 11-24-2009 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.

Bodyglide Anti Chafe Balm 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

Active Ingredient:

Allantoin 0.5%


Skin Protectant


  • Helps prevent and helps relieve chafed, chapped or cracked skinhelps protect from the drying effects of wind and cold weather


For external use only.

When Using This Product

  • Do not get into eyes

Stop Use And Ask A Doctor If

  • Condition worsenssymptoms last more than 7 days or clear up and occur again within a few days

Do Not Use On

  • Deep or puncture wounds animal bites serious burnsKeep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.


Apply as needed.

Inactive Ingredients

Aloe barbadensis extract, C18-36 acid triglycerides, caprylic/capric triglycerides, FD & C Red No. 40, tocopheryl acetate, tribeheninQuestions +1 425.467.6580Distributor: Bodyglide, Bellevue, WA USA©2009 W Sternoff LLC, Bellevue, WA USAAll rights reserved www.bodyglide.comTrademarks registered Made in Canada

* Please review the disclaimer below.