BODYGLIDE ANTI CHAFE BALM- allantoin stick

Bodyglide anti chafe balm by

Drug Labeling and Warnings

Bodyglide anti chafe balm by is a Otc medication manufactured, distributed, or labeled by W STERNOFF LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Active Ingredient: 

Allantoin 0.5%

Purpose

Skin Protectant

Uses

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

Warnings

For external use only.

When using this product

• do not get into eyes

Stop use and ask a doctor if

• condition worsens
  
• symptoms 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 burns

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

INGREDIENTS AND APPEARANCE

BODYGLIDE ANTI CHAFE BALM 
allantoin stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 15197-007
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: 15197-007-07	2 g in 1 TUBE
2	NDC: 15197-007-14	1 in 1 PACKAGE
2	NDC: 15197-007-13	36.9 g in 1 TUBE
3	NDC: 15197-007-26	1 in 1 PACKAGE
3	NDC: 15197-007-25	70 g in 1 TUBE
4	NDC: 15197-007-46	1 in 1 PACKAGE
4	NDC: 15197-007-45	12.8 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)