FDA.reportPublic FDA data

Coppertone Oil Free SPF 50 Sunscreen

Product NDC
66800-4094
11-digit product format
668004094
Labeler code
66800
Product ID
66800-4094_47460679-8962-b4d5-e063-6394a90ab919
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3%, Homosalate 10%, Octisalate 4.5%, Octocrylene 8%
Dosage form
LOTION
Route
TOPICAL
Labeler
Beiersdorf Inc
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-04-01
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 10; 4.5; 8 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 Oil Free SPF 50 Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100g
HOMOSALATE10 g/100g
OCTISALATE4.5 g/100g
OCTOCRYLENE8 g/100g

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66800-4094-3Coppertone Oil Free SPF 50 Sunscreen88 g in 1 TUBELOTION884

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66800-4094COPPERTONE OIL FREE SPF 50 SUNSCREEN (AVOBENZONE 3%, HOMOSALATE 10%, OCTISALATE 4.5%, OCTOCRYLENE 8%) LOTION [BEIERSDORF INC]3Current NDC, Legacy NDC, 1 package rows20250115_ded1f158-36d1-153f-e053-2995a90ace30.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66800-4094-36680040940388 g in 1 TUBE (66800-4094-3) 88 g2022-04-010000-00-00NoNoCurrent