- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
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WARNINGS
Warnings: For external use only 1. In case of having following symptoms after using this product, stop using it immediately. If the symptoms get worse, you need to consult a dermatologist. 1) In case of having problems such as red spots, swelling, itching or irritation during using this product 2) In case of having the same symptoms above on the part where you put this product, which is exposed to direct sunlight. 2. Do not use it on the part where you have a scar, eczema or dermatitis. 3. Topical use only 4. Keep out of reach of children
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Direction
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RAPHAGEN POWDE R
allantoin powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71125-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) Allantoin 0.007 g in 0.7 g Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) Arginine (UNII: 94ZLA3W45F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71125-100-02 10 in 1 CARTON 10/01/2017 1 NDC:71125-100-01 0.7 g in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 10/01/2017 Labeler - RAPHAGEN CO. LTD (689852157) Registrant - RAPHAGEN CO. LTD (689852157) Establishment Name Address ID/FEI Business Operations RAPHAGEN CO. LTD 689852157 manufacture(71125-100)