Home NDC 51672-2115-00 NDC 51672-2115-00 - Feverall Childrens This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 51672-2115
Requested NDC 51672-2115-00
Package NDCs from labels 51672-2115-0, 51672-2115-2, 51672-2115-4, 51672-2115-00
Manufacturer Sun Pharmaceutical Industries, Inc. | Cosette Pharmaceuticals NC Laboratories, LLC
Effective date 2026-08-24
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Feverall ® Children's Sun Pharmaceutical Industries, Inc. | Cosette Pharmaceuticals NC Laboratories, LLC 2026-08-24 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51672-2115-0 Feverall Childrens 1 in 1 BLISTER PACK SUPPOSITORY 1 7 51672-2115-2 Feverall Childrens 6 in 1 CARTON SUPPOSITORY 6 7 51672-2115-4 Feverall Childrens 50 in 1 CARTON SUPPOSITORY 50 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51672-2115 FEVERALL CHILDRENS (ACETAMINOPHEN) SUPPOSITORY [TARO PHARMACEUTICALS U.S.A. INC.] 6 Current NDC, Legacy NDC, 3 package rows 20241211_861e2987-5473-45b0-b2a6-f980a9b0e809.zip
DailyMed Socrata Ingredients# 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 56 of 150 · 2,999 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.