CLARINS BROAD SPECTRUM SPF 50 Sunscreen Body

Product NDC
58668-9922
11-digit product format
586689922
Labeler code
58668
Product ID
58668-9922_0bbf07bd-4010-4f2a-e063-6294a90a1ed4
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE,
Dosage form
CREAM
Route
TOPICAL
Labeler
Laboratoires Clarins
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-01-01
Substance
AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 100; 75; 50; 100 mg/mL; 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
CLARINS BROAD SPECTRUM SPF 50 Sunscreen Body
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE100 mg/mL
OCTINOXATE75 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE100 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4Y5P7MUD51, 4X49Y0596W, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58668-9922-1CLARINS BROAD SPECTRUM SPF 50 Sunscreen Body150 mL in 1 BOTTLECREAM1501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58668-9922CLARINS BROAD SPECTRUM SPF 50 SUNSCREEN BODY (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE,) CREAM [LABORATOIRES CLARINS]1Current NDC, 1 package rows20240101_7feb0679-6557-4917-a386-7ce2c14a94e2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
58668-9922-158668992201150 mL in 1 BOTTLE (58668-9922-1) 150 ml2024-01-01NoNoHistorical