Dr. C. Tuna Sunscreen 50 SPF UVA UVB Protection Face and Body Sun

Product NDC
74690-006
11-digit product format
746900006
Labeler code
74690
Product ID
74690-006_47f546a1-56ae-7ba4-e063-6294a90a9a27
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE
Dosage form
LOTION
Route
TOPICAL
Labeler
Farmasi US LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-01-08
Substance
AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTOCRYLENE
Active strength
25; 80; 65; 90 mg/mL; mg/mL; 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. C. Tuna Sunscreen 50 SPF UVA UVB Protection Face and Body Sun
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE25 mg/mL
HOMOSALATE80 mg/mL
OCTINOXATE65 mg/mL
OCTOCRYLENE90 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4Y5P7MUD51, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74690-006-01Dr. C. Tuna Sunscreen 50 SPF UVA UVB Protection Face and Body Sun75 mL in 1 TUBELOTION754

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74690-006DR. C. TUNA SUNSCREEN 50 SPF UVA UVB PROTECTION FACE AND BODY SUN (AVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE) LOTION [FARMASI US LLC]3Current NDC, Legacy NDC, 1 package rows20231213_27fdbd2b-60de-4906-a176-5c5198d9925b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
74690-006-017469000060175 mL in 1 TUBE (74690-006-01) 75 ml2020-01-080000-00-00NoNoCurrent