Sunscreen

Product NDC
41250-714
11-digit product format
412500714
Labeler code
41250
Product ID
41250-714_4b344d6f-13a9-e374-e063-6394a90a73c2
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
Meijer, Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-07-02
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30.3; 101; 50.5; 101 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sunscreen
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30.3 mg/mL
HOMOSALATE101 mg/mL
OCTISALATE50.5 mg/mL
OCTOCRYLENE101 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41250-714-21Sunscreen89 mL in 1 TUBELOTION8915
41250-714-34Sunscreen236 mL in 1 BOTTLE, PLASTICLOTION23615

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41250-714SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [MEIJER DISTRIBUTION, INC]13Current NDC, Legacy NDC, 2 package rows20250216_e9f4a2bb-d21e-4b38-9a37-23c23c8ad857.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
41250-714-214125007142189 mL in 1 TUBE89 mlHistorical
41250-714-3441250071434236 mL in 1 BOTTLE, PLASTIC (41250-714-34) 236 ml2019-07-02NoNoCurrent