GoodSense SPF 30 Sunscreen

Product NDC
50804-221
11-digit product format
508040221
Labeler code
50804
Product ID
50804-221_42a42d17-d6f3-bbcd-e063-6394a90a1945
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 10%
Dosage form
LOTION
Route
TOPICAL
Labeler
Geiss, Destin, & Dunn, Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-10-21
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 10; 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 30 Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100mL
HOMOSALATE10 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
50804-221-04GoodSense SPF 30 Sunscreen118 mL in 1 BOTTLE, PLASTICLOTION1184

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50804-221GOODSENSE SPF 30 SUNSCREEN (AVOBENZONE 3%, HOMOSALATE 10%, OCTISALATE 5%, OCTOCRYLENE 10%) LOTION [GEISS, DESTIN, & DUNN, INC.]3Current NDC, Legacy NDC, 1 package rows20241217_c23c754a-9441-0a05-e053-2995a90afc55.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50804-221-0450804022104118 mL in 1 BOTTLE, PLASTIC (50804-221-04) 118 ml2019-10-210000-00-00NoNoCurrent