NDC 15197-009 Bodyglide For Her
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 15197 - W Sternoff Llc
- 15197-009 - Bodyglide For Her
Product Packages
NDC Code 15197-009-81
Package Description: 1 TUBE in 1 PACKAGE / 22.68 g in 1 TUBE (15197-009-80)
Product Details
What is NDC 15197-009?
What are the uses for Bodyglide For Her?
Which are Bodyglide For Her UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Bodyglide For Her Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- ALOE (UNII: V5VD430YW9)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".