BODYGLIDE FOR HER- allantoin stick

Bodyglide For Her by

Drug Labeling and Warnings

Bodyglide For Her 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
  
• temporarily protects minor cuts, scrapes, burns

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

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)

INGREDIENTS AND APPEARANCE

BODYGLIDE FOR HER 
allantoin stick

Product 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)