NDC | 58264-0059-1 |
Set ID | b153cf23-eb3b-4647-b7f4-44380d498334 |
Category | HUMAN OTC DRUG LABEL |
Packager | DNA Labs, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- 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
D-59
fucus vesiculosus, spongia officinalis skeleton, roasted, graphite, oyster shell calcium carbonate, crude, sodium sulfate, and croton oil solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0059 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Fucus vesiculosus (UNII: 535G2ABX9M) (Fucus vesiculosus - UNII:535G2ABX9M) Fucus vesiculosus 3 [hp_X] in 1 mL Spongia officinalis skeleton, roasted (UNII: 1PIP394IID) (Spongia officinalis skeleton, roasted - UNII:1PIP394IID) Spongia officinalis skeleton, roasted 3 [hp_X] in 1 mL Graphite (UNII: 4QQN74LH4O) (Graphite - UNII:4QQN74LH4O) Graphite 12 [hp_X] in 1 mL Oyster shell calcium carbonate, crude (UNII: 2E32821G6I) (Oyster shell calcium carbonate, crude - UNII:2E32821G6I) Oyster shell calcium carbonate, crude 12 [hp_X] in 1 mL Sodium sulfate (UNII: 0YPR65R21J) (Sodium sulfate anhydrous - UNII:36KCS0R750) Sodium sulfate 2 [hp_X] in 1 mL Croton oil (UNII: WK97EQG57S) (Croton oil - UNII:WK97EQG57S) Croton oil 4 [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:58264-0059-1 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)