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NDC 73162-0001-01 Fat Loss Activation Complex 4; 4; 2; 8; 8; 8; 8; 4; 2 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details
Fat Loss Activation Complex 4; 4; 2; 8; 8; 8; 8; 4; 2 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Fat Loss Activation Complex is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Health Masters LLC. The primary component is AGAVE AMERICANA LEAF; CAPSICUM; FUCUS VESICULOSUS; GOLD; GRAPHITE; IRON; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; POTASSIUM CARBONATE.
Product Information
| NDC | 73162-0001 |
|---|---|
| Product ID | 73162-0001_09ad71e3-a245-4ebe-921e-5cccf2692b3e |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Fat Loss Activation Complex |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Fucus Vesiculosus, Kali Carbonicum, Agave Americana, Capsicum Annuum, Phytolacca Decandra, Aurum Metallicum, Calcarea Carbonica, Ferrum Metallicum, Graphites |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LIQUID |
| Route | ORAL |
| Active Ingredient Strength | 4; 4; 2; 8; 8; 8; 8; 4; 2 |
| Active Ingredient Units | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Substance Name | AGAVE AMERICANA LEAF; CAPSICUM; FUCUS VESICULOSUS; GOLD; GRAPHITE; IRON; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; POTASSIUM CARBONATE |
| Labeler Name | Health Masters LLC |
| Pharmaceutical Class | Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant All |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | n/a |
Package
NDC 73162-0001-01 (73162000101)
| NDC Package Code | 73162-0001-1 |
|---|---|
| Billing NDC | 73162000101 |
| Package | 30 mL in 1 BOTTLE, DROPPER (73162-0001-1) |
| Marketing Start Date | 2020-02-26 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |