FDA.reportPublic FDA data

Coppertone Complete Sunscreen SPF 50

Product NDC
66800-0030
11-digit product format
668000030
Labeler code
66800
Product ID
66800-0030_4746f16c-c5c5-8eb4-e063-6294a90afe9d
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3%, Homosalate 9%, Octisalate 4.5%, Octocrylene 9%
Dosage form
LOTION
Route
TOPICAL
Labeler
Beiersdorf Inc
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-11-02
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 9; 4.5; 9 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 Complete Sunscreen SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100g
HOMOSALATE9 g/100g
OCTISALATE4.5 g/100g
OCTOCRYLENE9 g/100g

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66800-0030-7Coppertone Complete Sunscreen SPF 50207 g in 1 TUBELOTION2077

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66800-0030COPPERTONE COMPLETE SUNSCREEN SPF 50 (AVOBENZONE 3%, HOMOSALATE 9%, OCTISALATE 4.5%, OCTOCRYLENE 9%) LOTION [BEIERSDORF INC]5Current NDC, Legacy NDC, 1 package rows20241207_d473e7ed-4a9f-76fe-e053-2995a90ab37d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66800-0030-766800003007207 g in 1 TUBE (66800-0030-7) 207 g2021-11-020000-00-00NoNoCurrent