Label: T-10- malus pumila whole solution
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Contains inactivated NDC Code(s)
NDC Code(s): 58264-0255-1 - Packager: DNA Labs, Inc.
- Category: HUMAN OTC DRUG LABEL
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 19, 2022
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- SPL UNCLASSIFIED SECTION
- INDICATIONS
- INGREDIENTS
- SUGGESTED DOSAGE
- STORAGE AND HANDLING
- Warnings
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
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INGREDIENTS AND APPEARANCE
T-10
malus pumila whole solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0255 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MALUS PUMILA WHOLE (UNII: 04W636S1V3) (MALUS PUMILA WHOLE - UNII:04W636S1V3) MALUS PUMILA WHOLE 30 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58264-0255-1 29.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/01/1990 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/1990 Labeler - DNA Labs, Inc. (031784339) Establishment Name Address ID/FEI Business Operations RNA Bio/Pharma, Inc 883081523 manufacture(58264-0255)