Label: D17- naja naja whole, scrophularia nodosa, lactic acid, dl-, and radium bromide solution
- NDC Code(s): 58264-0017-1
- 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 June 2, 2022
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INGREDIENTS AND APPEARANCE
D17
naja naja whole, scrophularia nodosa, lactic acid, dl-, and radium bromide solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0017 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NAJA NAJA WHOLE (UNII: D279BDR31E) (NAJA NAJA WHOLE - UNII:D279BDR31E) NAJA NAJA WHOLE 30 [hp_X] in 1 mL SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (SCROPHULARIA NODOSA - UNII:7H443NUB2T) SCROPHULARIA NODOSA 2 [hp_X] in 1 mL LACTIC ACID, DL- (UNII: 3B8D35Y7S4) (LACTIC ACID, DL- - UNII:3B8D35Y7S4) LACTIC ACID, DL- 4 [hp_X] in 1 mL RADIUM BROMIDE (UNII: R74O7T8569) (RADIUM CATION - UNII:05456MVL7T) RADIUM BROMIDE 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:58264-0017-1 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)