Search by Drug Name or NDC

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

Package Images

NDC 69780-0006-01 (69780000601)

Pricing Information	N/A
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

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

ACTIVE INGREDIENTS:

Fucus Vesiculosus 2X, Kali Carbonicum 2X, Agave Americana 4X, Capsicum Annuum 4X, Phytolacca Decandra 4X, Aurum Metallicum 8X, Calcarea Carbonica 8X, Ferrum Metallicum 8X, Graphites 8X.

INDICATIONS:

For temporary relief of symptoms related to increased appetite, regulation of fat metabolism, headache, fatigue and detoxification stress.

WARNINGS:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: Sealed for your protection. Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

10 drops under the tongue, 3 to 6 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

For temporary relief of symptoms related to increased appetite, regulation of fat metabolism, headache, fatigue and detoxification stress.

INACTIVE INGREDIENTS:

Demineralized water, 25% ethanol.

QUESTIONS:

Dist. by:

True Weight Loss Solutions

6102 Shallowford Road

Chattanooga, TN 37421

PACKAGE LABEL DISPLAY:

True

weightloss

solutions

FAT LOSS

ACTIVATION

COMPLEX

Homeopathic

1 FL OZ (30 ml)

NDC #: 69780-0006-1

INGREDIENTS AND APPEARANCE

FAT LOSS ACTIVATION COMPLEX

fucus vesiculosus, kali carbonicum, agave americana, capsicum annuum, phytolacca decandra, aurum metallicum, calcarea carbonica, ferrum metallicum, graphites liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69780-0006
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69780-0006-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	07/17/2018	09/21/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		07/17/2018	09/21/2023

Labeler - True Weight Loss Solutions (079796575)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(69780-0006) , api manufacture(69780-0006) , label(69780-0006) , pack(69780-0006)

Revised: 1/2022

Document Id: f8018b89-b07b-47b1-a8cf-42cf60da3331

Set id: f0ceeef3-0b2d-489a-80c7-d69782523a54

Version: 3

Effective Time: 20220119

Search by Drug Name or NDC

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

Product Information

Package

Package Images

NDC 69780-0006-01 (69780000601)

Contents

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

ACTIVE INGREDIENTS:

INDICATIONS:

WARNINGS:

KEEP OUT OF REACH OF CHILDREN:

DIRECTIONS:

INDICATIONS:

INACTIVE INGREDIENTS:

QUESTIONS:

PACKAGE LABEL DISPLAY:

INGREDIENTS AND APPEARANCE

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