Naturium UV Reflect Antioxidant SPF 50

Product NDC
76354-125
11-digit product format
763540125
Labeler code
76354
Product ID
76354-125_43962032-3b0d-8369-e063-6294a90ae5fc
Type
HUMAN OTC DRUG
Nonproprietary name
Homosalate, Octisalate, Avobenzone
Dosage form
LOTION
Route
TOPICAL
Labeler
e.l.f. Cosmetics, Inc
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-04-10
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength
30; 100; 50 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
Naturium UV Reflect Antioxidant SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE100 mg/mL
OCTISALATE50 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76354-125-01Naturium UV Reflect Antioxidant SPF 501 in 1 CARTONLOTION13
76354-125-01Naturium UV Reflect Antioxidant SPF 5050 mL in 1 TUBELOTION503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76354-125NATURIUM UV REFLECT ANTIOXIDANT SPF 50 (HOMOSALATE, OCTISALATE, AVOBENZONE) LOTION [E.L.F. COSMETICS, INC]2Current NDC, 2 package rows20241212_0a5c6fc8-6cdc-0ae5-e063-6394a90ae01c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
76354-125-01763540125011 TUBE in 1 CARTON (76354-125-01) / 50 mL in 1 TUBE1 tube2023-04-10NoNoHistorical