Label: FAT LOSS ACTIVATION COMPLEX- fucus vesiculosus, kali carbonicum, agave americana, capsicum annuum, phytolacca decandra, aurum metallicum, calcarea carbonica, ferrum metallicum, graphites liquid
- NDC Code(s): 73162-0001-1
- Packager: Health Masters LLC
- 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 April 6, 2023
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- ACTIVE INGREDIENTS:
- INDICATIONS:
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INGREDIENTS AND APPEARANCE
FAT LOSS ACTIVATION COMPLEX
fucus vesiculosus, kali carbonicum, agave americana, capsicum annuum, phytolacca decandra, aurum metallicum, calcarea carbonica, ferrum metallicum, graphites liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73162-0001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 2 [hp_X] in 1 mL POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 2 [hp_X] in 1 mL AGAVE AMERICANA LEAF (UNII: 8511ZMP5QK) (AGAVE AMERICANA LEAF - UNII:8511ZMP5QK) AGAVE AMERICANA LEAF 4 [hp_X] in 1 mL CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG) CAPSICUM 4 [hp_X] in 1 mL PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG) PHYTOLACCA AMERICANA ROOT 4 [hp_X] in 1 mL GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 8 [hp_X] in 1 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X] in 1 mL IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON 8 [hp_X] in 1 mL GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 8 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73162-0001-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 02/26/2020 02/26/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/26/2020 02/26/2025 Labeler - Health Masters LLC (115005283) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(73162-0001) , api manufacture(73162-0001) , label(73162-0001) , pack(73162-0001)