Vivant Day Treatment SPF 15

Product NDC
63750-015
11-digit product format
637500015
Labeler code
63750
Product ID
63750-015_26322aba-bc7d-2fa5-e063-6394a90a1e72
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate 7.50% Octisalate 5.00%
Dosage form
LOTION
Route
TOPICAL
Labeler
Vivant Pharmaceuticals, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-02-01
Substance
OCTINOXATE; OCTISALATE
Active strength
7.5; 5 g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Vivant Day Treatment SPF 15
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTINOXATE7.5 g/100mL
OCTISALATE5 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4Y5P7MUD51, 4X49Y0596W

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63750-015-03Vivant Day Treatment SPF 1589 mL in 1 BOTTLELOTION892

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63750-015VIVANT DAY TREATMENT SPF 15 (OCTINOXATE 7.50% OCTISALATE 5.00%) LOTION [VIVANT PHARMACEUTICALS, LLC]2Current NDC, 1 package rows20241107_10a95d0a-366f-0611-e063-6294a90abb44.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
63750-015-036375000150389 mL in 1 BOTTLE (63750-015-03) 89 ml2024-02-01NoNoCurrent