Home NDC 41250-362 MEIJER KIDS BROAD SPECTRUM SPF 50 MINERAL BASED SUNSCREEN
Product NDC 41250-362
11-digit product format 412500362
Labeler code 41250
Product ID 41250-362_249b0894-c5a1-5135-e063-6394a90a3ef6
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, OCTISALATE, ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler MEIJER DISTRIBUTION INC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-11-06
Substance ZINC OXIDE; OCTISALATE; OCTINOXATE
Active strength 145; 50; 75 mg/mL; mg/mL; mg/mL
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 MEIJER KIDS BROAD SPECTRUM SPF 50 MINERAL BASED SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 145 mg/mL OCTISALATE 50 mg/mL OCTINOXATE 75 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 4X49Y0596W Internal UNII lookup 4Y5P7MUD51 Internal UNII 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 41250-362-71 MEIJER KIDS BROAD SPECTRUM SPF 50 MINERAL BASED SUNSCREEN 177 mL in 1 BOTTLE LOTION 177 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-362 MEIJER KIDS BROAD SPECTRUM SPF 50 MINERAL BASED SUNSCREEN (OCTINOXATE, OCTISALATE, ZINC OXIDE) LOTION [MEIJER DISTRIBUTION INC] 4 Current NDC, Legacy NDC, 1 package rows 20241018_a9f4fd45-3bbb-14a7-e053-2995a90ab28f.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 26 of 357 · 7,139 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 41250-362-71 41250036271 177 mL in 1 BOTTLE (41250-362-71) 177 ml 2018-11-06 0000-00-00 No No Current