What is NDC 73162-0004?

73162-0004 is the product NDC for Fat Loss Activation Complex, Fucus vesiculosus 2 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Health Masters LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Fat Loss Activation Complex (Fucus Vesiculosus, Kali Carbonicum, Asafoetida, Capsicum Annuum, Phytolacca Decandra, Aurum Metallicum, Calcarea Carbonica, Ferrum Metallicum, Graphites).

What is the active ingredient?

Fucus vesiculosus, Potassium carbonate, Ferula assa-foetida resin, Capsicum, Phytolacca americana root, Gold, Oyster shell calcium carbonate, Crude, Iron, Graphite.

Health Masters LLC, NDC labeler code 73162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Fat Loss Activation Complex?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Fat Loss Activation Complex NDC 73162-0004

NDC codes

FDA NDC Directory

Product NDC (as listed)73162-0004Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73162-0004Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
73162-0004-1	7316200040173162000401	30 mL in 1 BOTTLE, DROPPER (73162-0004-1)Marketed from Apr 6, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Fat Loss Activation Complex
Generic name (nonproprietary): fucus vesiculosus, kali carbonicum, asafoetida, capsicum annuum, phytolacca decandra, aurum metallicum, calcarea carbonica, ferrum metallicum, graphites
Active ingredients: Fucus vesiculosus — 2 [hp_X]/mLPotassium carbonate — 2 [hp_X]/mLFerula assa-foetida resin — 4 [hp_X]/mLCapsicum — 4 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLGold — 8 [hp_X]/mLOyster shell calcium carbonate, Crude — 8 [hp_X]/mLIron — 8 [hp_X]/mLGraphite — 8 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Health Masters LLCNDC labeler code 73162
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 6, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 73162-0004_72ab052d-a89b-482b-989e-b754918bb79eSPL ID 72ab052d-a89b-482b-989e-b754918bb79eSPL set ID 61fc35d1-007e-4e9d-af6e-be2869a44997UNII 535G2ABX9M, BQN1B9B9HA, W9FZA51AS1, 00UK7646FG, 11E6VI8VEG, 79Y1949PYO, 2E32821G6I, E1UOL152H7, 4QQN74LH4O
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Standardized Chemical Allergen

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N473162000401 followed by a unit qualifier and the quantity

Package 73162-0004-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Apr 6, 2023.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73162-0004

What is NDC 73162-0004?: 73162-0004 is the product NDC for Fat Loss Activation Complex, Fucus vesiculosus 2 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Health Masters LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Fat Loss Activation Complex (Fucus Vesiculosus, Kali Carbonicum, Asafoetida, Capsicum Annuum, Phytolacca Decandra, Aurum Metallicum, Calcarea Carbonica, Ferrum Metallicum, Graphites).
What is the active ingredient?: Fucus vesiculosus, Potassium carbonate, Ferula assa-foetida resin, Capsicum, Phytolacca americana root, Gold, Oyster shell calcium carbonate, Crude, Iron, Graphite.
Who is the labeler?: Health Masters LLC, NDC labeler code 73162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Fat Loss Activation Complex?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.