Dr. C. Tuna Sun Bronzing Oil SPF 6

Product NDC
74690-014
11-digit product format
746900014
Labeler code
74690
Product ID
74690-014_09735fbf-7779-ca3f-e063-6294a90a9f94
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE
Dosage form
OIL
Route
TOPICAL
Labeler
Farmasi US LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-07-25
Substance
OCTINOXATE
Active strength
35 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Dr. C. Tuna Sun Bronzing Oil SPF 6
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTINOXATE35 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4Y5P7MUD51

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
baf7f49c-75b6-496b-a00e-8e766a8e4f03Product name120210127
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74690-014-01Dr. C. Tuna Sun Bronzing Oil SPF 6115 mL in 1 BOTTLEOIL1152
74690-014-01Dr. C. Tuna Sun Bronzing Oil SPF 61 in 1 BOXOIL12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74690-014DR. C. TUNA SUN BRONZING OIL SPF 6 (OCTINOXATE) OIL [FARMASI US LLC]2Current NDC, Legacy NDC, 2 package rows20231106_91b428cc-1c80-4d56-8450-790c66de4133.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
74690-014-01746900014011 BOTTLE in 1 BOX (74690-014-01) / 115 mL in 1 BOTTLE1 bottle2021-07-250000-00-00NoNoCurrent