LUMO Booz Hangover Companiion

Product NDC
81425-003
11-digit product format
814250003
Labeler code
81425
Product ID
81425-003_22f0d1d8-f6ab-4a1e-85e3-30c3826c660b
Type
HUMAN OTC DRUG
Nonproprietary name
Chininum arsenicosum, Natrum phosphoricum, Nux voomica, Vespa crabro
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
Applied Bioenergetics, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-10-15
Substance
QUININE ARSENITE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRYCHNOS NUX-VOMICA SEED; VESPA CRABRO
Active strength
30; 30; 30; 30 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
Pharmacologic classes
Allergens [CS], Antimalarial [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
42QO5P0NLMQUININE ARSENITEQUININE ARSENITE
70WT22SF4BSODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE7782-85-6SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
269XH13919STRYCHNOS NUX-VOMICA SEED8046-97-7STRYCHNOS NUX-VOMICA SEED
K3ALM8S49HVESPA CRABROVESPA CRABRO

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
81425-003-1081425000310180 TABLET, CHEWABLE in 1 BOTTLE (81425-003-10) 2023-10-15NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LUMO-e Booz Hangover CompaniionApplied Bioenergetics, LLC2025-11-10HUMAN OTC DRUG LABEL4
LUMO-e Booz Hangover CompaniionApplied Bioenergetics, LLC2024-12-31HUMAN OTC DRUG LABEL3