Label: WATERROK FULVIC ACID- fulvic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 82236-0001-1 - Packager: Waterrok Co., Ltd.
- 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 September 10, 2021
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- Download DRUG LABEL INFO: PDF XML
- 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
WATERROK FULVIC ACID
fulvic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82236-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FULVIC ACID (UNII: XII14C5FXV) (FULVIC ACID - UNII:XII14C5FXV) FULVIC ACID 0.6 mg in 1000 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82236-0001-1 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/11/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/11/2021 Labeler - Waterrok Co., Ltd. (694099609) Registrant - Waterrok Co., Ltd. (694099609) Establishment Name Address ID/FEI Business Operations Waterrok Co., Ltd. 694099609 manufacture(82236-0001)
