- SPL UNCLASSIFIED SECTION
- INDICATIONS
- ACTIVE INGREDIENT
- RX CAUTION
- SUGGESTED DOSAGE
- STORAGE AND HANDLING
- Warnings
- PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
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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)