Label: D-67 (ammonium carbonate, hydrogen cyanide, camphor- natural, activated charcoal, crotalus durissus terrificus venom, tobacco leaf, veratrum album root, and spigelia anthelmia solution
- NDC Code(s): 58264-0067-1
- Packager: DNA Labs, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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 January 13, 2025
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INGREDIENTS AND APPEARANCE
D-67
ammonium carbonate, hydrogen cyanide, camphor (natural), activated charcoal, crotalus durissus terrificus venom, tobacco leaf, veratrum album root, and spigelia anthelmia solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0067 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (CARBONATE ION - UNII:7UJQ5OPE7D) AMMONIUM CARBONATE 6 [hp_X] in 1 mL HYDROGEN CYANIDE (UNII: 2WTB3V159F) (HYDROGEN CYANIDE - UNII:2WTB3V159F) HYDROGEN CYANIDE 6 [hp_X] in 1 mL CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 4 [hp_X] in 1 mL ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 30 [hp_X] in 1 mL CROTALUS DURISSUS TERRIFICUS VENOM (UNII: 2XF6I0446G) (CROTALUS DURISSUS TERRIFICUS VENOM - UNII:2XF6I0446G) CROTALUS DURISSUS TERRIFICUS VENOM 12 [hp_X] in 1 mL TOBACCO LEAF (UNII: 6YR2608RSU) (TOBACCO LEAF - UNII:6YR2608RSU) TOBACCO LEAF 6 [hp_X] in 1 mL VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (VERATRUM ALBUM ROOT - UNII:QNS6W5US1Z) VERATRUM ALBUM ROOT 4 [hp_X] in 1 mL SPIGELIA ANTHELMIA (UNII: WYT05213GE) (SPIGELIA ANTHELMIA - UNII:WYT05213GE) SPIGELIA ANTHELMIA 6 [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:58264-0067-1 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)