Label: KENAF WET WIPE KIDS- allantoin liquid
- NDC Code(s): 72944-0004-1
- Packager: MEDICELL BIO CO., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 9, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
1. For external use only.
1) Do not use over the wound and irritated skin with eczema or infections
2) Discontinue using the product if signs of irritations and/or rashes occur and seek professional medical help
2. Keep the cover closed tight after use
3. Do not put the left over contents back into the container to avoid deterioration
1) Avoid contact with eyes
2) Keep out of reach of children
3) Store in a cool and dry place, away from direct sun light
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KENAF WET WIPE KIDS
allantoin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72944-0004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.05 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72944-0004-1 190 g in 1 POUCH; Type 0: Not a Combination Product 04/09/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/09/2017 Labeler - MEDICELL BIO CO., Ltd. (689843703) Registrant - MEDICELL BIO CO., Ltd. (689843703) Establishment Name Address ID/FEI Business Operations MEDICELL BIO CO., Ltd. 689843703 manufacture(72944-0004)
