ULTA FACE SPF 30

Product NDC
62296-8292
11-digit product format
622968292
Labeler code
62296
Product ID
62296-8292_d45165d4-d9aa-427b-b338-0512db3b2a4e
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Dosage form
LOTION
Route
TOPICAL
Labeler
Ulta
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-08-17
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength
2; 13; 5; 2; 4 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
ULTA FACE SPF 30
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE2 g/100g
HOMOSALATE13 g/100g
OCTISALATE5 g/100g
OCTOCRYLENE2 g/100g
OXYBENZONE4 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM, 95OOS7VE0Y

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62296-8292-2ULTA FACE SPF 3088 g in 1 BOTTLELOTION881

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62296-8292ULTA FACE SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [ULTA]1Current NDC, Legacy NDC, 1 package rows20160519_78ed84b3-5dda-4792-83cd-86f63846fef7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62296-8292-26229682920288 g in 1 BOTTLE (62296-8292-2) 88 g2016-05-190000-00-00NoNoCurrent