FDA.reportPublic FDA data

Dr. Throwers SPF 30 Face and Body Sunscreen

Product NDC
72839-605
11-digit product format
728390605
Labeler code
72839
Product ID
72839-605_29a70b32-1d8e-858d-e063-6394a90a9c78
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3%, Homosalate 12%, Octisalate 5%, Octocrylene 3%
Dosage form
LOTION
Route
TOPICAL
Labeler
Derma Care Research Labs, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-09-28
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 12; 5; 3 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
Dr. Throwers SPF 30 Face and Body Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100g
HOMOSALATE12 g/100g
OCTISALATE5 g/100g
OCTOCRYLENE3 g/100g

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72839-605-02Dr. Throwers SPF 30 Face and Body Sunscreen57 g in 1 BOTTLE, PLASTICLOTION572

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72839-605DR. THROWERS SPF 30 FACE AND BODY SUNSCREEN (AVOBENZONE 3%, HOMOSALATE 12%, OCTISALATE 5%, OCTOCRYLENE 3%) LOTION [DERMA CARE RESEARCH LABS, LLC]2Current NDC, Legacy NDC, 1 package rows20241222_d680b6f6-e1a9-47a4-e053-2a95a90ae3b0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72839-605-027283906050257 g in 1 BOTTLE, PLASTIC (72839-605-02) 57 g2021-09-280000-00-00NoNoCurrent