Fat Loss Activation Complex

Product NDC

73162-0001

11-digit product format

731620001

Labeler code

73162

Product ID

73162-0001_78ebd535-82bb-4326-b992-85aa928fa4e5

Type

HUMAN OTC DRUG

Nonproprietary name

Fucus Vesiculosus, Kali Carbonicum, Agave Americana, Capsicum Annuum, Phytolacca Decandra, Aurum Metallicum, Calcarea Carbonica, Ferrum Metallicum, Graphites

Dosage form

LIQUID

Route

ORAL

Labeler

Health Masters LLC

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2020-02-26

Marketing end

0000-00-00

Substance

AGAVE AMERICANA LEAF; CAPSICUM; FUCUS VESICULOSUS; GOLD; GRAPHITE; IRON; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; POTASSIUM CARBONATE

Active strength

4 [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

Pharmacologic classes

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 Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC], Vegetable Proteins [CS]

NDC exclude flag

No

Listing certified through

2023-12-31

Current FDA listing

Historical FDA.report record