FDA.reportPublic FDA data

QC SPF 50 Sunscreen

Product NDC
63868-531
11-digit product format
638680531
Labeler code
63868
Product ID
63868-531_295784a9-db54-649d-e063-6294a90a6a4b
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%
Dosage form
LOTION
Route
TOPICAL
Labeler
CDMA
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-12-22
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 15; 5; 10 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
QC SPF 50 Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

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

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63868-531-08QC SPF 50 Sunscreen227 g in 1 BOTTLE, PLASTICLOTION2272
63868-531-18QC SPF 50 Sunscreen227 g in 1 BOTTLE, PLASTICLOTION2272

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63868-531QC SPF 50 SUNSCREEN (AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%) LOTION [CDMA]2Current NDC, 2 package rows20241217_f82080b1-ef90-a027-e053-6294a90a19f2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
63868-531-0863868053108227 g in 1 BOTTLE, PLASTIC (63868-531-08) 227 g2021-12-22NoNoCurrent
63868-531-1863868053118227 g in 1 BOTTLE, PLASTIC (63868-531-18) 227 g2021-12-22NoNoCurrent