FDA.reportPublic FDA data

Coppertone Limited Edition Sunscreen SPF 30

Product NDC
66800-3026
11-digit product format
668003026
Labeler code
66800
Product ID
66800-3026_47461e3c-c6de-1d6e-e063-6294a90a51ae
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 2%, Homosalate 8%, Octisalate 4.5%, Octocrylene 7%
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Beiersdorf Inc
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-11-01
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
2; 8; 4.5; 7 g/100g; g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Coppertone Limited Edition Sunscreen SPF 30
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE2 g/100g
HOMOSALATE8 g/100g
OCTISALATE4.5 g/100g
OCTOCRYLENE7 g/100g

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66800-3026-5Coppertone Limited Edition Sunscreen SPF 30156 g in 1 CANAEROSOL, SPRAY1563

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66800-3026COPPERTONE LIMITED EDITION SUNSCREEN SPF 30 (AVOBENZONE 2%, HOMOSALATE 8%, OCTISALATE 4.5%, OCTOCRYLENE 7%) AEROSOL, SPRAY [BEIERSDORF INC]2Current NDC, 1 package rows20250112_f41e09bf-407d-65a4-e053-2a95a90a2436.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
66800-3026-566800302605156 g in 1 CAN (66800-3026-5) 156 g2022-11-01NoNoHistorical