Label: VIRX-H- naja naja tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 69792-000-01 - Packager: Medforce Solutions Inc.
- 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 May 14, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VIRX-H
naja naja tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69792-000 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM) NAJA NAJA VENOM 10 [hp_X] Inactive Ingredients Ingredient Name Strength CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) ORANGE OIL (UNII: AKN3KSD11B) SUCROSE (UNII: C151H8M554) THIMEROSAL (UNII: 2225PI3MOV) Product Characteristics Color white Score no score Shape ROUND Size 5mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69792-000-01 15 in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/13/2015 Labeler - Medforce Solutions Inc. (051523866) Establishment Name Address ID/FEI Business Operations Medforce Solutions Inc. 051523866 manufacture(69792-000)