Sunscreen Glowing, SPF 30

Product NDC
70000-0280
11-digit product format
700000280
Labeler code
70000
Product ID
70000-0280_473c89aa-8347-37fa-e063-6294a90afd0a
Type
HUMAN OTC DRUG
Nonproprietary name
Sunscreen Glowing Lotion
Dosage form
LOTION
Route
TOPICAL
Labeler
Cardinal Health, Inc
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-12-14
Marketing end
2026-12-19
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
1.5; 4.5; 2.5; 3.5 g/50mL; g/50mL; g/50mL; g/50mL
NDC exclude flag
No
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sunscreen Glowing, SPF 30

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HOMOSALATE1.5 g/50mL
OCTOCRYLENE4.5 g/50mL
AVOBENZONE2.5 g/50mL
OCTISALATE3.5 g/50mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiV06SV4M95S, 5A68WGF6WM, G63QQF2NOX, 4X49Y0596W

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70000-0280-1Sunscreen Glowing, SPF 3050 mL in 1 BOTTLELOTION503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70000-0280SUNSCREEN GLOWING, SPF 30 (SUNSCREEN GLOWING LOTION) LOTION [CARDINAL HEALTH, INC]1Current NDC, 1 package rows20241215_28ed3b60-1139-f657-e063-6394a90a52fa.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70000-0280-17000002800150 mL in 1 BOTTLE (70000-0280-1) 50 ml2024-12-142026-12-19NoNoHistorical