Label: BODYGLIDE FOR HER- allantoin stick
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Contains inactivated NDC Code(s)
NDC Code(s): 15197-009-80, 15197-009-81 - Packager: W STERNOFF LLC
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 12, 2009
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- SPL UNCLASSIFIED SECTION
- Active Ingredient:
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Do not use on
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- Inactive Ingredients
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INGREDIENTS AND APPEARANCE
BODYGLIDE FOR HER
allantoin stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:15197-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 5 mg in 1 g Inactive Ingredients Ingredient Name Strength ALOE (UNII: V5VD430YW9) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) TRIBEHENIN (UNII: 8OC9U7TQZ0) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:15197-009-81 1 in 1 PACKAGE 1 NDC:15197-009-80 22.68 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part347 11/24/2009 Labeler - W STERNOFF LLC (006801828)