BODYGLIDE FOR HER- allantoin stick 
W STERNOFF LLC

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.

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Bodyglide For Her

Active Ingredient: 

Allantoin 0.5%

Purpose

Skin Protectant

Uses

Warnings

For external use only.

When using this product

Stop use and ask a doctor if

Do not use on

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions

Apply as needed.

Inactive Ingredients

aloe barbadensis extract, C18-36 acid triglycerides, caprylic/capric triglycerides, FD & C Red No. 40, tocopheryl acetate, tribehenin

Questions +1 425.467.6580

Distributor: Bodyglide, Bellevue, WA USA

Made in Canada

Principal Display Panel

BODYGLIDE®

For Her

anti-chafe stick

balm

dry, non-greasy skin lubricant

helps prevent & relieve chafed skin
also great for chapped, cracked & dry skin

bras, thighs, feet

apply before activity or anytime

petroleum & oil free

no mess

NET WT. 0.80 oz (22.68 g)

Principal Display Panel BODYGLIDE® For Her anti-chafe stick balm dry, non-greasy skin lubricant helps prevent & relieve chafed skin also great for chapped, cracked & dry skin bras, thighs, feet apply before activity or anytime petroleum & oil free no mess NET WT. 0.80 oz (22.68 g)

BODYGLIDE FOR HER 
allantoin stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15197-009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:15197-009-811 in 1 PACKAGE
1NDC:15197-009-8022.68 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34711/24/2009
Labeler - W STERNOFF LLC (006801828)

Revised: 12/2009
Document Id: 6f13950d-4373-49f7-9faf-5de9ec64b0cf
Set id: fa716980-803d-4d33-8fce-ee7aa6da0830
Version: 1
Effective Time: 20091212
 
W STERNOFF LLC