ULTRA SOOTHING TONER- allantoin liquid 
Dermafirm 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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Drug Facts

Allantoin

Water, Glycerin

Skin protectant

Soothing

keep out of reach of the children

After cleansing, soak it in a cotton swab and use it as if you wipe it out carefully.

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

for external use only


label

ULTRA SOOTHING TONER 
allantoin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71638-0008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71638-0008-1200 mL in 1 BOTTLE; Type 0: Not a Combination Product09/04/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34709/04/2017
Labeler - Dermafirm INC. (690171603)
Registrant - Dermafirm INC. (690171603)
Establishment
NameAddressID/FEIBusiness Operations
Dermafirm INC.690171603label(71638-0008) , pack(71638-0008) , manufacture(71638-0008)

Revised: 9/2017
Document Id: 58569429-5db3-3bcb-e053-2a91aa0abb87
Set id: 58569429-5db2-3bcb-e053-2a91aa0abb87
Version: 1
Effective Time: 20170904
 
Dermafirm INC.