Home NDC 72988-0034 NOVOMINSYRUP
Product NDC 72988-0034
11-digit product format 729880034
Labeler code 72988
Product ID 72988-0034_f2e9f62e-22fb-9555-e053-2995a90ae44b
Type HUMAN OTC DRUG
Nonproprietary name Caffeine Anhydrous, Meclizine Hydrochloride Hydrate, Pyridoxine Hydrochloride
Dosage form LIQUID
Route ORAL
Labeler Lydia Co., Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2023-01-23
Substance CAFFEINE; MECLIZINE HYDROCHLORIDE; PYRIDOXINE HYDROCHLORIDE
Active strength 20; 25; 5 mg/6mL; mg/6mL; mg/6mL
Pharmacologic classes Analogs/Derivatives [Chemical/Ingredient], Antiemetic [EPC], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Emesis Suppression [PE], Methylxanthine [EPC], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Xanthines [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base NOVOMINSYRUP
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAFFEINE 20 mg/6mL MECLIZINE HYDROCHLORIDE 25 mg/6mL PYRIDOXINE HYDROCHLORIDE 5 mg/6mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3G6A5W338E Internal UNII lookup HDP7W44CIO Internal UNII lookup 68Y4CF58BV Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72988-0034-1 NOVOMINSYRUP 6 mL in 1 POUCH LIQUID 6 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72988-0034 NOVOMINSYRUP (CAFFEINE ANHYDROUS, MECLIZINE HYDROCHLORIDE HYDRATE, PYRIDOXINE HYDROCHLORIDE) LIQUID [LYDIA CO., LTD.] 1 Current NDC, 1 package rows 20230124_f2e9fbc8-501f-c386-e053-2995a90a6a14.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 Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join NOVOMINSYRUP CAFFEINE ANHYDROUS, MECLIZINE HYDROCHLORIDE HYDRATE, PYRIDOXINE HYDROCHLORIDE Lydia Co., Ltd. f2e9fbc8-501f-c386-e053-2995a90a6a14 2023-01-23 Warnings Exact identifier ndc (product): 72988-0034
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72988-0034-1 72988003401 6 mL in 1 POUCH (72988-0034-1) 6 ml 2023-01-23 No No Current