FDA.reportPublic FDA data

Chemical Sunscreen SPF50

Product NDC
60232-0043
11-digit product format
602320043
Labeler code
60232
Product ID
60232-0043_42c3d5f5-5ddb-4f54-9843-59d438639624
Type
HUMAN OTC DRUG
Nonproprietary name
octisalate, avobenzone, homosalate, octocrylene sunscreen
Dosage form
SPRAY
Route
TOPICAL
Labeler
Swiss-American CDMO, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-03-29
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 150; 50; 100 g/1000g; g/1000g; g/1000g; g/1000g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Chemical Sunscreen SPF50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 g/1000g
HOMOSALATE150 g/1000g
OCTISALATE50 g/1000g
OCTOCRYLENE100 g/1000g

Harmonized Identifiers#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
124351b2-6dbf-42d0-9ea7-f0e299215f9aProduct name120210115
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60232-0043-1Chemical Sunscreen SPF5090 g in 1 BOTTLE, SPRAYSPRAY902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60232-0043CHEMICAL SUNSCREEN SPF50 (OCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE SUNSCREEN) SPRAY [SWISS-AMERICAN CDMO, LLC]2Current NDC, 1 package rows20240509_50f47495-93aa-4e11-a153-d4c847a36c99.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
60232-0043-16023200430190 g in 1 BOTTLE, SPRAY (60232-0043-1) 90 g2024-03-29NoNoCurrent