BODYGLIDE ANTI CHAFE BALM- 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.

----------

Anti-chafe balm

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

©2009 W Sternoff LLC, Bellevue, WA USA

All rights reserved www.bodyglide.com
Trademarks registered

Made in Canada

Principal Display Panel

BODYGLIDE
anti-chafe balm

Dry, Non-Greasy

helps prevent & relieve

hot spots, chafing, rubbing

feet, mid body, upper body

shoes & all footwear, thighs, saddle sores, bras, under arms
great for daily use

trusted by endurance athletes

sweat & water resistant

Invisible, No Oils, Many apply it just once, Remove with soap and water, Recommended for compression wear, neoprene and wetsuits

Principal Display Panel BODYGLIDE anti-chafe balm Dry, Non-Greasy

BODYGLIDE ANTI CHAFE BALM 
allantoin stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15197-007
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:15197-007-072 g in 1 TUBE
2NDC:15197-007-141 in 1 PACKAGE
2NDC:15197-007-1336.9 g in 1 TUBE
3NDC:15197-007-261 in 1 PACKAGE
3NDC:15197-007-2570 g in 1 TUBE
4NDC:15197-007-461 in 1 PACKAGE
4NDC:15197-007-4512.8 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: b6537332-c86e-4fec-8d8b-568f387277c4
Set id: 05bac498-5d1b-4329-9c06-0cc59f9c8d8e
Version: 1
Effective Time: 20091210
 
W STERNOFF LLC