sunscreen

Product NDC
79481-0938
11-digit product format
794810938
Labeler code
79481
Product ID
79481-0938_4b96fe9a-18cf-e15c-e063-6394a90aa2b1
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form
SPRAY
Route
TOPICAL
Labeler
Meijer, Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-01-27
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 150; 50; 80 mg/g; mg/g; mg/g; mg/g
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 mg/g
HOMOSALATE150 mg/g
OCTISALATE50 mg/g
OCTOCRYLENE80 mg/g

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-0938-1sunscreen156 g in 1 CANSPRAY1568
79481-0938-2sunscreen258 g in 1 CANSPRAY2588

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79481-0938SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [MEIJER DISTRIBUTION, INC]7Current NDC, Legacy NDC, 2 package rows20250403_8f5e634c-765b-4ffe-bb12-753d64c90cf9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79481-0938-179481093801156 g in 1 CAN (79481-0938-1) 156 g2021-01-270000-00-00NoNoCurrent
79481-0938-279481093802258 g in 1 CAN (79481-0938-2) 258 g2021-01-270000-00-00NoNoCurrent