GoodSense SPF 50 Sunscreen

Product NDC
50804-083
11-digit product format
508040083
Labeler code
50804
Product ID
50804-083_432f2e03-aad3-735a-e063-6294a90a511c
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%
Dosage form
LOTION
Route
TOPICAL
Labeler
Geiss, Destin, & Dunn, Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-06-12
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 15; 5; 10 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
GoodSense SPF 50 Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100mL
HOMOSALATE15 g/100mL
OCTISALATE5 g/100mL
OCTOCRYLENE10 g/100mL

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50804-083-08GoodSense SPF 50 Sunscreen237 mL in 1 BOTTLE, PLASTICLOTION2374

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50804-083GOODSENSE SPF 50 SUNSCREEN (AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%) LOTION [GEISS, DESTIN, & DUNN, INC.]3Current NDC, Legacy NDC, 1 package rows20241217_c85d59a1-6ae1-bb2e-e053-2995a90af20e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50804-083-0850804008308237 mL in 1 BOTTLE, PLASTIC (50804-083-08) 237 ml2020-06-120000-00-00NoNoCurrent