FDA.reportPublic FDA data

Black Girl Sunscreen SPF 30

Product NDC
72839-121
11-digit product format
728390121
Labeler code
72839
Product ID
72839-121_29a4feca-c288-51cb-e063-6294a90a264a
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 8%
Dosage form
SPRAY
Route
TOPICAL
Labeler
Derma Care Research Labs, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-01-03
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 15; 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
Black Girl Sunscreen SPF 30
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100g
HOMOSALATE15 g/100g
OCTISALATE5 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
72839-121-03Black Girl Sunscreen SPF 3085 g in 1 CANSPRAY852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72839-121BLACK GIRL SUNSCREEN SPF 30 (AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 8%) SPRAY [DERMA CARE RESEARCH LABS, LLC]2Current NDC, Legacy NDC, 1 package rows20241222_d438be95-0f88-69d7-e053-2995a90a982e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72839-121-037283901210385 g in 1 CAN (72839-121-03) 85 g2022-01-030000-00-00NoNoCurrent