KONEUK SUNSCREEN SPF50

Product NDC
84167-323
11-digit product format
841670323
Labeler code
84167
Product ID
84167-323_48dd7f6e-2a4e-2c92-e063-6294a90a4255
Type
HUMAN OTC DRUG
Nonproprietary name
KONEUK SUNSCREEN SPF50
Dosage form
CREAM
Route
CUTANEOUS
Labeler
Guangzhou Meixi Biotechnology Co., Ltd.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-01-21
Substance
AVOBENZONE; ENSULIZOLE; HOMOSALATE; OCTOCRYLENE; TITANIUM DIOXIDE
Active strength
1; 1; 1; 1; 1 g/1; g/1; g/1; g/1; g/1
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
KONEUK SUNSCREEN SPF50
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE1 g/1
ENSULIZOLE1 g/1
HOMOSALATE1 g/1
OCTOCRYLENE1 g/1
TITANIUM DIOXIDE1 g/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, 9YQ9DI1W42, V06SV4M95S, 5A68WGF6WM, 15FIX9V2JP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84167-323-03KONEUK SUNSCREEN SPF505 in 1 BOXCREAM51
84167-323-03KONEUK SUNSCREEN SPF501 in 1 BOTTLECREAM11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84167-323-03841670323035 BOTTLE in 1 BOX (84167-323-03) / 1 CREAM in 1 BOTTLE5 bottle2026-01-21NoNoHistorical