Medication Guide App

Bodyglide For Her

Dosage form: stick
Ingredients: ALLANTOIN 5mg in 1g
Labeler: W STERNOFF LLC
NDC Code: 15197-009

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.

Bodyglide For Her

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)

BODYGLIDE FOR HER 
allantoin stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15197-009
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (ALLANTOIN) ALLANTOIN5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALOE 
.ALPHA.-TOCOPHEROL ACETATE, D- 
TRIBEHENIN 
MEDIUM-CHAIN TRIGLYCERIDES 
FD&C RED NO. 40 
Packaging
#Item CodePackage Description
1NDC:15197-009-811 TUBE (1 TUBE) 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
 
W STERNOFF LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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