Label: ALKALINE SUPER IONIZED WATER spray
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Contains inactivated NDC Code(s)
NDC Code(s): 41768-001-01 - Packager: Foshan Eric Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated June 8, 2020
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- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- ACTIVE INGREDIENT
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- PURPOSE
- WARNINGS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALKALINE SUPER IONIZED WATER
alkaline super ionized water sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41768-001 Route of Administration EXTRACORPOREAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 0.17 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41768-001-01 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/09/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/09/2020 Labeler - Foshan Eric Biotechnology Co., Ltd. (417683769) Establishment Name Address ID/FEI Business Operations Foshan Eric Biotechnology Co., Ltd. 417683769 manufacture(41768-001)