Label: EXODEN CURE POWDER- aluminum chlorohydroxy allantoinate powder
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NDC Code(s):
70602-004-01,
70602-004-02,
70602-004-03,
70602-004-04, view more70602-004-05, 70602-004-06
- Packager: LIFEON Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated March 9, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EXODEN CURE POWDER
aluminum chlorohydroxy allantoinate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70602-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCLOXA (UNII: 18B8O9DQA2) (ALLANTOIN - UNII:344S277G0Z) ALCLOXA 0.16 g in 100 g Inactive Ingredients Ingredient Name Strength BENTONITE (UNII: A3N5ZCN45C) SODIUM CHLORIDE (UNII: 451W47IQ8X) XYLITOL (UNII: VCQ006KQ1E) LEVOMENTHOL (UNII: BZ1R15MTK7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70602-004-02 1 in 1 CARTON 03/09/2021 1 NDC:70602-004-01 10 g in 1 POUCH; Type 0: Not a Combination Product 2 NDC:70602-004-04 1 in 1 CARTON 03/09/2021 2 NDC:70602-004-03 30 g in 1 CONTAINER; Type 0: Not a Combination Product 3 NDC:70602-004-06 1 in 1 CARTON 03/09/2021 3 NDC:70602-004-05 70 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 unapproved drug other 03/09/2021 Labeler - LIFEON Corp. (688528872) Registrant - LIFEON Corp. (688528872) Establishment Name Address ID/FEI Business Operations Korea Shidenta 688171734 manufacture(70602-004)