TOPCARE EVERYDAY ULTRA PROTECTION SPF 50

Product NDC
36800-132
11-digit product format
368000132
Labeler code
36800
Product ID
36800-132_2487db4b-bc34-acfe-e063-6394a90a9e20
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form
LOTION
Route
TOPICAL
Labeler
TOPCO ASSOCIATES LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2014-02-11
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 100; 45; 80 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
TOPCARE EVERYDAY ULTRA PROTECTION SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE100 mg/mL
OCTISALATE45 mg/mL
OCTOCRYLENE80 mg/mL

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
36800-132-11TOPCARE EVERYDAY ULTRA PROTECTION SPF 50237 mL in 1 BOTTLELOTION2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
36800-132TOPCARE EVERYDAY ULTRA PROTECTION SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [TOPCO ASSOCIATES LLC]2Current NDC, Legacy NDC, 1 package rows20241017_c5601d22-2353-7319-e053-2a95a90a16c0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
36800-132-1136800013211237 mL in 1 BOTTLE (36800-132-11) 237 ml2014-02-110000-00-00NoNoCurrent