DR.JART EVERY SUN DAY MINERAL SUN SCREEN

Product NDC
49404-153
11-digit product format
494040153
Labeler code
49404
Product ID
49404-153_47ed472b-224a-5b9a-e063-6394a90a7030
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium dioxide, Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Have & Be Co., Ltd.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-12-22
Substance
TITANIUM DIOXIDE; ZINC OXIDE
Active strength
41; 115 mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
DR.JART EVERY SUN DAY MINERAL SUN SCREEN
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TITANIUM DIOXIDE41 mg/mL
ZINC OXIDE115 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii15FIX9V2JP, SOI2LOH54Z

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49404-153-01DR.JART EVERY SUN DAY MINERAL SUN SCREEN1 in 1 CARTONCREAM15
49404-153-01DR.JART EVERY SUN DAY MINERAL SUN SCREEN50 mL in 1 TUBECREAM505
49404-153-02DR.JART EVERY SUN DAY MINERAL SUN SCREEN5 mL in 1 TUBECREAM55

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49404-153DR.JART EVERY SUN DAY MINERAL SUN SCREEN (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [HAVE & BE CO., LTD.]4Current NDC, Legacy NDC, 3 package rows20241227_f06c31b4-da5f-6495-e053-2995a90ae67c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49404-153-01494040153011 TUBE in 1 CARTON (49404-153-01) / 50 mL in 1 TUBE1 tube2022-12-220000-00-00NoNoCurrent
49404-153-02494040153025 mL in 1 TUBE (49404-153-02) 5 ml2022-12-220000-00-00NoNoCurrent