Home NDC 55741-600 Doans
Product NDC 55741-600
11-digit product format 557410600
Labeler code 55741
Product ID 55741-600_ce3b4271-d310-414e-d7c1-dea98afe2670
Type HUMAN OTC DRUG
Nonproprietary name Magnesium salicylate
Dosage form TABLET
Route ORAL
Labeler Dr. Reddy's Laboratories Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-05-24
Substance MAGNESIUM SALICYLATE
Active strength 580 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
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 Doans
Brand name suffix Maximum Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM SALICYLATE 580 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 41728CY7UX Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198742 Internal RxNorm lookup 830388 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55741-600-01 Doans Maximum Strength 1 in 1 CARTON TABLET 1 3 55741-600-01 Doans Maximum Strength 100 in 1 BOTTLE TABLET 100 3 55741-600-30 Doans Maximum Strength 30 in 1 BOTTLE TABLET 30 3 55741-600-30 Doans Maximum Strength 1 in 1 CARTON TABLET 1 3 55741-600-34 Doans Maximum Strength 8 in 1 BLISTER PACK TABLET 8 3 55741-600-34 Doans Maximum Strength 3 in 1 CARTON TABLET 3 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55741-600 DOANS MAXIMUM STRENGTH (MAGNESIUM SALICYLATE) TABLET [DR. REDDY'S LABORATORIES INC.] 2 Current NDC, 6 package rows 20241109_c906df41-bb45-03ea-b1a8-2b9816d55c97.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 39 of 79 · 1,579 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 55741-600-01 55741060001 1 BOTTLE in 1 CARTON (55741-600-01) / 100 TABLET in 1 BOTTLE 1 bottle 2025-02-01 No No Current 55741-600-30 55741060030 1 BOTTLE in 1 CARTON (55741-600-30) / 30 TABLET in 1 BOTTLE 1 bottle 2026-05-01 No No Current 55741-600-34 55741060034 3 BLISTER PACK in 1 CARTON (55741-600-34) / 8 TABLET in 1 BLISTER PACK 3 blister pack 2025-02-01 No No Current