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; OCTOCRYLENE; OCTISALATE; OXYBENZONE
Active strength: 2; 13; 2; 5; 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

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: ULTA FACE SPF 30
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
AVOBENZONE	2 g/100g
HOMOSALATE	13 g/100g
OCTOCRYLENE	2 g/100g
OCTISALATE	5 g/100g
OXYBENZONE	4 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
G63QQF2NOX	Internal UNII lookup
V06SV4M95S	Internal UNII lookup
5A68WGF6WM	Internal UNII lookup
4X49Y0596W	Internal UNII lookup
95OOS7VE0Y	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
78ed84b3-5dda-4792-83cd-86f63846fef7	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62296-8292-2	ULTA FACE SPF 30	88 g in 1 BOTTLE	LOTION	88		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62296-8292	ULTA FACE SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [ULTA]	1	Current NDC, Legacy NDC, 1 package rows	20160519_78ed84b3-5dda-4792-83cd-86f63846fef7.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ULTA FACE SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE	Ulta	78ed84b3-5dda-4792-83cd-86f63846fef7	2016-05-19	Warnings	Exact identifier ndc (product): 62296-8292

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
95OOS7VE0Y	OXYBENZONE	131-57-7	OXYBENZONE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
62296-8292-2	62296829202	88 g in 1 BOTTLE (62296-8292-2)	88 g	2016-05-19	0000-00-00	No	No	Current