Dr. C. Tuna Sun Face and Body SPF 50

Product NDC
74690-015
11-digit product format
746900015
Labeler code
74690
Product ID
74690-015_09735b2f-2ae4-ca91-e063-6294a90a210a
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
2021-07-25
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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Dr. C. Tuna Sun Face and Body SPF 50
Listing expiration
2026-12-31

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
74690-015-01Dr. C. Tuna Sun Face and Body SPF 501 in 1 BOXLOTION12
74690-015-01Dr. C. Tuna Sun Face and Body SPF 5075 mL in 1 BOTTLELOTION752

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74690-015DR. C. TUNA SUN FACE AND BODY SPF 50 (AVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE) LOTION [FARMASI US LLC]2Current NDC, Legacy NDC, 2 package rows20231106_141f9d22-deb7-4b6b-97b5-ee21898b96f7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
74690-015-01746900015011 BOTTLE in 1 BOX (74690-015-01) / 75 mL in 1 BOTTLE1 bottle2021-07-250000-00-00NoNoCurrent