FDA.reportPublic FDA data

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

Additional Listing Data#

Finished product
Yes
Brand name base
LUMO Booz Hangover Companiion
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
QUININE ARSENITE30 [hp_C]/1
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE30 [hp_C]/1
STRYCHNOS NUX-VOMICA SEED30 [hp_C]/1
VESPA CRABRO30 [hp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
42QO5P0NLMInternal UNII lookup
70WT22SF4BInternal UNII lookup
269XH13919Internal UNII lookup
K3ALM8S49HInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8e23e541-2c78-4ca0-a61a-ad110665c7f3Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
22bca8fc-c2b1-897d-b515-117a7522ccaeProduct name320150731
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81425-003-10LUMO Booz Hangover Companiion180 in 1 BOTTLETABLET, CHEWABLE1804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81425-003LUMO BOOZ HANGOVER COMPANIION (CHININUM ARSENICOSUM, NATRUM PHOSPHORICUM, NUX VOOMICA, VESPA CRABRO) TABLET, CHEWABLE [APPLIED BIOENERGETICS, LLC]3Current NDC, 1 package rows20250101_8e23e541-2c78-4ca0-a61a-ad110665c7f3.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LUMO Booz Hangover CompaniionCHININUM ARSENICOSUM, NATRUM PHOSPHORICUM, NUX VOOMICA, VESPA CRABROApplied Bioenergetics, LLC8e23e541-2c78-4ca0-a61a-ad110665c7f32025-11-10WarningsExact identifier
ndc (product): 81425-003

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
81425-003-1081425000310180 TABLET, CHEWABLE in 1 BOTTLE (81425-003-10) 2023-10-15NoNoCurrent