FDA.reportPublic FDA data

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
OCTINOXATE; OCTISALATE; ZINC OXIDE
Active strength
75; 50; 145 mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
MEIJER KIDS BROAD SPECTRUM SPF 50 MINERAL BASED SUNSCREEN
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTINOXATE75 mg/mL
OCTISALATE50 mg/mL
ZINC OXIDE145 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4Y5P7MUD51, 4X49Y0596W, SOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41250-362-71MEIJER KIDS BROAD SPECTRUM SPF 50 MINERAL BASED SUNSCREEN177 mL in 1 BOTTLELOTION1774

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41250-362MEIJER KIDS BROAD SPECTRUM SPF 50 MINERAL BASED SUNSCREEN (OCTINOXATE, OCTISALATE, ZINC OXIDE) LOTION [MEIJER DISTRIBUTION INC]4Current NDC, Legacy NDC, 1 package rows20241018_a9f4fd45-3bbb-14a7-e053-2995a90ab28f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41250-362-7141250036271177 mL in 1 BOTTLE (41250-362-71) 177 ml2018-11-060000-00-00NoNoCurrent