NOVOMINSYRUP

Manufacturer
Lydia Co., Ltd.
Effective date
2023-01-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:53:26

Label at a glance#

ProductNOVOMINSYRUP
Active ingredientCAFFEINE, MECLIZINE HYDROCHLORIDE, PYRIDOXINE HYDROCHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Caffeine Anhydrous, Meclizine Hydrochloride Hydrate, Pyridoxine Hydrochloride

OTC - PURPOSE SECTION

■ throw up■ whirl ■ headache

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

■ adult and children 15 years of age and older: 1 pack 30 minutes before boarding.

■ children under 15 years of age: ask a doctor

WARNINGS SECTION

Ask a doctor before use if you have taking a prescription drug.

When using this product

■ Do not take more than 3 pack in 24 hours

■ If you take an additional dose, take it after 4 hours or more

Keep out of reach of children

INACTIVE INGREDIENT SECTION

concentrated glycerin, malt syrup, high fructose 55

DOSAGE & ADMINISTRATION SECTION

for oral use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CAFFEINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
MECLIZINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
PYRIDOXINE Pharmacologic Class Indexing1Indexing - Pharmacologic Class20170310

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
ac6963c4-31c6-325f-ee58-83a0a06597adProduct name520221206
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
5e18e798-5614-cf5c-0185-38b1cb77a093Product name220160822
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72988-0034-1NOVOMINSYRUP6 mL in 1 POUCHLIQUID61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72988-0034NOVOMINSYRUP (CAFFEINE ANHYDROUS, MECLIZINE HYDROCHLORIDE HYDRATE, PYRIDOXINE HYDROCHLORIDE) LIQUID [LYDIA CO., LTD.]1Current NDC, 1 package rows20230124_f2e9fbc8-501f-c386-e053-2995a90a6a14.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72988-003472988-0034-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

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
NOVOMINSYRUPCAFFEINE ANHYDROUS, MECLIZINE HYDROCHLORIDE HYDRATE, PYRIDOXINE HYDROCHLORIDELydia Co., Ltd.f2e9fbc8-501f-c386-e053-2995a90a6a142023-01-23WarningsExact identifier
ndc (package): 72988-0034-1
ndc (product): 72988-0034
ndc11 (package): 72988003401
spl id: f2e9f62e-22fb-9555-e053-2995a90ae44b
spl set id: f2e9fbc8-501f-c386-e053-2995a90a6a14

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.