NDC codes

FDA NDC Directory
Product NDC (as listed)81425-003Labeler and product segments. Claims need a package NDC.
Product NDC at billing width81425-0003Add 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 NDC11-digit (billing)PackageCopy
81425-003-108142500031081425000310180 TABLET, CHEWABLE in 1 BOTTLE (81425-003-10)Marketed from Oct 15, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
LUMO Booz Hangover Companiion
Generic name (nonproprietary)
chininum arsenicosum, natrum phosphoricum, nux voomica, vespa crabro
Active ingredients
Quinine arsenite — 30 [hp_C]/1Sodium phosphate, Dibasic, Heptahydrate — 30 [hp_C]/1Strychnos nux-vomica seed — 30 [hp_C]/1Vespa crabro — 30 [hp_C]/1
Dosage form
Tablet, Chewable
Route
Oral
Labeler
Applied Bioenergetics, LLCNDC labeler code 81425
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
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 81425-003_22f0d1d8-f6ab-4a1e-85e3-30c3826c660bSPL ID 22f0d1d8-f6ab-4a1e-85e3-30c3826c660bSPL set ID 8e23e541-2c78-4ca0-a61a-ad110665c7f3UNII 42QO5P0NLM, 70WT22SF4B, 269XH13919, K3ALM8S49H
Pharmacologic class
Antimalarial; 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

N481425000310 followed by a unit qualifier and the quantity

Package 81425-0003-10. 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 .

Indications (excerpt from the label)

Uses* Temporarily Relieves Minor and Occasional: • headache • hyperacidity • heartburn • sour belching • gas • nausea • symptoms of hangover • motion sickness • irritable • dizziness

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 81425-003

What is NDC 81425-003?
81425-003 is the product NDC for LUMO Booz Hangover Companiion, Quinine arsenite 30 [hp_C]/1 + 3 more ingredients tablet, chewable, listed with the FDA by Applied Bioenergetics, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
LUMO Booz Hangover Companiion (Chininum arsenicosum, Natrum phosphoricum, Nux voomica, Vespa crabro).
What is the active ingredient?
Quinine arsenite, Sodium phosphate, Dibasic, Heptahydrate, Strychnos nux-vomica seed, Vespa crabro.
Who is the labeler?
Applied Bioenergetics, LLC, NDC labeler code 81425. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for LUMO Booz Hangover Companiion?
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.

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