Gblv HP NDC 43406-0613

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0613Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0613Add 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
43406-0613-1	43406061301	30 mL in 1 BOTTLE, DROPPER (43406-0613-1)Marketed from Jun 1, 2016

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): Gblv HP
Generic name (nonproprietary): atropa belladonna, berberis vulgaris root bark, milk thistle, chelidonium majus, citrullus colocynthis fruit pulp, dioscorea villosa tuber, goldenseal, lycopodium clavatum spore, sodium sulfate, strychnos nux-vomica seed, phosphorus, anemone pulsatilla, veratrum album root
Active ingredients: Atropa belladonna — 30 [hp_C]/mLBerberis vulgaris root bark — 30 [hp_C]/mLMilk thistle — 30 [hp_C]/mLChelidonium majus — 30 [hp_C]/mLCitrullus colocynthis fruit pulp — 30 [hp_C]/mLDioscorea villosa tuber — 30 [hp_C]/mLGoldenseal — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLSodium sulfate — 30 [hp_C]/mLStrychnos nux-vomica seed — 30 [hp_C]/mLPhosphorus — 30 [hp_C]/mLAnemone pulsatilla — 30 [hp_C]/mLVeratrum album root — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 1, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43406-0613_80fed459-9130-46b5-906d-b6d90be133caSPL ID 80fed459-9130-46b5-906d-b6d90be133caSPL set ID cff4d830-6696-4cde-9cd7-4ce55e28b54bUNII WQZ3G9PF0H, 1TH8Q20J0U, U946SH95EE, 7E889U5RNN, 23H32AOH17, IWY3IWX2G8, ZW3Z11D0JV, C88X29Y479, 0YPR65R21J, 269XH13919, 27YLU75U4W, I76KB35JEV, QNS6W5US1ZUPC 0877730004499
Pharmacologic class: Non-Standardized Plant Allergenic Extract

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

N443406061301 followed by a unit qualifier and the quantity

Package 43406-0613-01. 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 Dec 12, 2025.

Indications (excerpt from the label)

USES: Temporarily relieves flatulence, constipation, and belching.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)