Label: ROK FULVIC ACID- fulvic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 82236-0003-1 - Packager: Waterrok Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 17, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ROK FULVIC ACID
fulvic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82236-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FULVIC ACID (UNII: XII14C5FXV) (FULVIC ACID - UNII:XII14C5FXV) FULVIC ACID 1.45 g in 1000 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82236-0003-1 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/18/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/18/2021 Labeler - Waterrok Co., Ltd. (694099609) Registrant - Waterrok Co., Ltd. (694099609) Establishment Name Address ID/FEI Business Operations Waterrok Co., Ltd. 694099609 manufacture(82236-0003)