FDA.reportPublic FDA data

Arizona Sun SPF 45 Surfblok Sunscreen

Product NDC
61973-112
11-digit product format
619730112
Labeler code
61973
Product ID
61973-112_4f0c7348-d1c7-1e51-e063-6294a90aa591
Type
HUMAN OTC DRUG
Nonproprietary name
Sunscreen
Dosage form
SPRAY
Route
TOPICAL
Labeler
Arizona Sun Products
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-02-21
Substance
AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength
30; 100; 75; 50; 70; 50 mg/g; mg/g; mg/g; mg/g; mg/g; mg/g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Arizona Sun SPF 45 Surfblok Sunscreen
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/g
HOMOSALATE100 mg/g
OCTINOXATE75 mg/g
OCTISALATE50 mg/g
OCTOCRYLENE70 mg/g
OXYBENZONE50 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4Y5P7MUD51, 4X49Y0596W, 5A68WGF6WM, 95OOS7VE0Y

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61973-112-04Arizona Sun SPF 45 Surfblok Sunscreen120 g in 1 BOTTLESPRAY1202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61973-112ARIZONA SUN SPF 45 SURFBLOK SUNSCREEN (SUNSCREEN) SPRAY [ARIZONA SUN PRODUCTS]1Current NDC, 1 package rows20240223_11e76815-9316-555d-e063-6294a90aeb81.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
61973-112-0461973011204120 g in 1 BOTTLE (61973-112-04) 120 g2024-02-21NoNoCurrent