Home NDC 10237-461 Zicam
Product NDC 10237-461
11-digit product format 102370461
Labeler code 10237
Product ID 10237-461_2081f496-df7b-4898-95fb-df19eca96a41
Type HUMAN OTC DRUG
Nonproprietary name Zinc Acetate Anhydrous, Zinc Gluconate, and Sambucus Nigra Flowering Top
Dosage form TABLET
Route ORAL
Labeler Church & Dwight Co., Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-04-30
Substance SAMBUCUS NIGRA FLOWERING TOP; ZINC ACETATE ANHYDROUS; ZINC GLUCONATE
Active strength 5; 2; 1 [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Copper Absorption Inhibitor [EPC], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Zicam
Brand name suffix Cold Remedy Rapidmelts Elderberry Citrus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC ACETATE ANHYDROUS 5 [hp_X]/1 ZINC GLUCONATE 2 [hp_X]/1 SAMBUCUS NIGRA FLOWERING TOP 1 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H2ZEY72PME Internal UNII lookup U6WSN5SQ1Z Internal UNII lookup CT03BSA18U Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10237-461-25 Zicam Cold Remedy Rapidmelts Elderberry Citrus 25 in 1 BOTTLE TABLET 25 2 10237-461-25 Zicam Cold Remedy Rapidmelts Elderberry Citrus 1 in 1 CARTON TABLET 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10237-461 ZICAM COLD REMEDY RAPIDMELTS ELDERBERRY CITRUS (ZINC ACETATE ANHYDROUS, ZINC GLUCONATE, AND SAMBUCUS NIGRA FLOWERING TOP) TABLET [CHURCH & DWIGHT CO., INC.] 2 Current NDC, Legacy NDC, 2 package rows 20240203_bbf1c8b7-56f8-ee7f-e053-2995a90a7b27.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 10237-461-25 10237046125 1 BOTTLE in 1 CARTON (10237-461-25) / 25 TABLET in 1 BOTTLE 1 bottle 2021-04-30 0000-00-00 No No Current