Sunscreen

Product NDC
11822-1013
11-digit product format
118221013
Labeler code
11822
Product ID
11822-1013_49da6e8b-bb25-2868-e063-6294a90a9bdf
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate,Otisalate, Octocrylene
Dosage form
SPRAY
Route
TOPICAL
Labeler
Rite Aid Corporation
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-12-06
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
90; 225; 250; 1000 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
AVOBENZONE90 mg/g
HOMOSALATE225 mg/g
OCTISALATE250 mg/g
OCTOCRYLENE1000 mg/g

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-1013-1Sunscreen156 g in 1 CANSPRAY1566

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-1013SUNSCREEN (AVOBENZONE, HOMOSALATE,OTISALATE, OCTOCRYLENE) SPRAY [RITE AID]4Current NDC, Legacy NDC, 1 package rows20240927_fe9146ec-b85d-43da-a391-377960f2c772.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-1013-111822101301156 g in 1 CAN (11822-1013-1) 156 g2021-12-060000-00-00NoNoCurrent