Nova Bright Skin SPF 30

Product NDC
72104-362
11-digit product format
721040362
Labeler code
72104
Product ID
72104-362_5a9283f7-8be2-4f48-bf51-bcfadb76ad7b
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Homosalate, Octisalate, Oxybenzone, Avobenzone
Dosage form
CREAM
Route
TOPICAL
Labeler
Innovation Brands Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-09-01
Substance
AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength
1.5; 6.2; 7.4; 5; 3.1 g/100g; g/100g; g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Nova Bright Skin SPF 30
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE1.5 g/100g
HOMOSALATE6.2 g/100g
OCTINOXATE7.4 g/100g
OCTISALATE5 g/100g
OXYBENZONE3.1 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4Y5P7MUD51, 4X49Y0596W, 95OOS7VE0Y

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72104-362-55Nova Bright Skin SPF 301 in 1 CARTONCREAM14
72104-362-55Nova Bright Skin SPF 3055 g in 1 JARCREAM554

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72104-362NOVA BRIGHT SKIN SPF 30 (OCTINOXATE, HOMOSALATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [LIONESSE USA, INC.]3Current NDC, Legacy NDC, 2 package rows20220811_1c201147-7a54-41b5-bdf0-394e3d7efc0c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72104-362-55721040362551 JAR in 1 CARTON (72104-362-55) / 55 g in 1 JAR1 jar2021-01-270000-00-00NoNoCurrent