NDC | 58264-0003-1 |
Set ID | 3cde4a8f-806a-4b23-8d49-b21150654f6d |
Category | HUMAN OTC DRUG LABEL |
Packager | DNA Labs, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- SPL UNCLASSIFIED SECTION
- INDICATIONS
- ACTIVE INGREDIENT
- RX CAUTION
- SUGGESTED DOSAGE
- STORAGE AND HANDLING
- Warnings
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
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INGREDIENTS AND APPEARANCE
D3
digitalis purpurea whole, strophanthus hispidus whole, crataegus mexicana whole, selenicereus grandiflorus whole, kalmia latifolia whole, arsenic trioxide, phosphorus, drimia maritima whole, spigelia anthelmia, and potassium carbonate solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0003 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGITALIS PURPUREA WHOLE (UNII: UD4O8TY7RW) (DIGITALIS PURPUREA WHOLE - UNII:UD4O8TY7RW) DIGITALIS PURPUREA WHOLE 4 [hp_X] in 1 mL STROPHANTHUS HISPIDUS WHOLE (UNII: W753F6AWFH) (STROPHANTHUS HISPIDUS WHOLE - UNII:W753F6AWFH) STROPHANTHUS HISPIDUS WHOLE 6 [hp_X] in 1 mL CRATAEGUS MEXICANA WHOLE (UNII: 09IF4Y848S) (CRATAEGUS MEXICANA WHOLE - UNII:09IF4Y848S) CRATAEGUS MEXICANA WHOLE 1 [hp_X] in 1 mL SELENICEREUS GRANDIFLORUS WHOLE (UNII: X8H7HS7MRM) (SELENICEREUS GRANDIFLORUS WHOLE - UNII:X8H7HS7MRM) SELENICEREUS GRANDIFLORUS WHOLE 2 [hp_X] in 1 mL KALMIA LATIFOLIA WHOLE (UNII: P1SWF7DK1Y) (KALMIA LATIFOLIA WHOLE - UNII:P1SWF7DK1Y) KALMIA LATIFOLIA WHOLE 3 [hp_X] in 1 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 5 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 5 [hp_X] in 1 mL DRIMIA MARITIMA WHOLE (UNII: UNM4C1735Z) (DRIMIA MARITIMA WHOLE - UNII:UNM4C1735Z) DRIMIA MARITIMA WHOLE 4 [hp_X] in 1 mL SPIGELIA ANTHELMIA (UNII: WYT05213GE) (SPIGELIA ANTHELMIA - UNII:WYT05213GE) SPIGELIA ANTHELMIA 3 [hp_X] in 1 mL POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 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:58264-0003-1 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)