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    NDC 69780-0006-01 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 True Weight Loss Solutions. 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 69780-0006
    Product ID 69780-0006_f8018b89-b07b-47b1-a8cf-42cf60da3331
    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 True Weight Loss Solutions
    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 69780-0006-01 (69780000601)

    NDC Package Code 69780-0006-1
    Billing NDC 69780000601
    Package 30 mL in 1 BOTTLE, DROPPER (69780-0006-1)
    Marketing Start Date 2018-07-17
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL f0ceeef3-0b2d-489a-80c7-d69782523a54 Details

    Revised: 1/2022