12 HOUR HEALING- allantoin ointment 
Skinfix, Inc.

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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Active Ingredients

Allantoin 0.5%

Purpose

Skin protectant

Uses

HELPS HEAL DRY, CHAPPED OR CRACKED SKIN. tEMPORARILY PROTECTS MINOR CUTS, SCRAPES, AND BURNS.

Warnings

For external use only.

When using this product

  • Avoid contact with eyes

WHEN USING THIS PRODUCT: AVOID CONTACT WITH EYES.

STOP USE AND ASK A DOCTOR IF

  • CONDITIONS WORSENS
  • SYMPTOMS LAST MORE THAN 7 DAYS OR CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS.

KEEP OUT OF REACH OF CHILDREN.

Directions

APPLY GENEROUSLY AS NEEDED TO IRRITATED OR AFFECTED SKIN.

OTHER INFORMATION

STORE AT 65 - 80°F. MAY STAIN FABRICS. FOR ADULTS AND CHILDREN TWO YEARS OF AGE AND OLDER.

Inactive Ingredients

Aloe Barbadensis Leaf Extract, Beeswax, Bisabolol, Butyrospermum Parkii (Shea) Butter, Cocos Nucifera (Coconut) Oil, Helianthus Annuus (Sunflower) Seed Oil, Petrolatum, Rosa Canina Fruit Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Cupuacu (Theobroma Grandiflorum) Seed Butter, Tocopherol.

Skinfix_12HR_US_4oz_V6_OL_R

12 HOUR HEALING 
allantoin ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61328-116
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
LEVOMENOL (UNII: 24WE03BX2T)  
SHEANUT OIL (UNII: O88E196QRF)  
COCONUT OIL (UNII: Q9L0O73W7L)  
THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
PETROLATUM (UNII: 4T6H12BN9U)  
ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)  
JOJOBA OIL (UNII: 724GKU717M)  
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61328-116-11102 g in 1 TUBE; Type 0: Not a Combination Product05/02/201701/03/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34705/02/201701/03/2020
Labeler - Skinfix, Inc. (203158183)
Registrant - Skinfix, Inc. (203158183)

Revised: 1/2020
 
Skinfix, Inc.