United States · FDA National Drug Code directory
LUMO Booz Hangover Companiion
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 81425-003_22f0d1d8-f6ab-4a1e-85e3-30c3826c660b
- Product NDC
- 81425-003
- Form
- TABLET, CHEWABLE
- Composition / generic term
- Chininum arsenicosum, Natrum phosphoricum, Nux voomica, Vespa crabro
- Labeler
- Applied Bioenergetics, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20231015
- Source listing expiry
- 20261231
Source-listed ingredients
- QUININE ARSENITE — 30 [hp_C]/1
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE — 30 [hp_C]/1
- STRYCHNOS NUX-VOMICA SEED — 30 [hp_C]/1
- VESPA CRABRO — 30 [hp_C]/1
These values do not establish equivalence or a dose recommendation.
Packages
- 180 TABLET, CHEWABLE in 1 BOTTLE (81425-003-10) · 81425-003-10
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →