SunPlus SPF 50 Everyday Inspired Broad Spectrum Sunscreen

Product NDC
84661-523
11-digit product format
846610523
Labeler code
84661
Product ID
84661-523_1fb55371-9455-49a4-e063-6394a90a4304
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, OCTISALATE, OCTOCRYLENE
Dosage form
LIQUID
Route
TOPICAL
Labeler
SUNPLUS SKIN CARE LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-08-05
Substance
AVOBENZONE; OCTISALATE; OCTOCRYLENE
Active strength
30; 50; 100 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
SunPlus SPF 50 Everyday Inspired Broad Spectrum Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE100 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, 4X49Y0596W, 5A68WGF6WM

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84661-523-00SunPlus SPF 50 Everyday Inspired Broad Spectrum Sunscreen177 mL in 1 CANLIQUID1771

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84661-523SUNPLUS SPF 50 EVERYDAY INSPIRED BROAD SPECTRUM SUNSCREEN (AVOBENZONE, OCTISALATE, OCTOCRYLENE) LIQUID [SUNPLUS SKIN CARE LLC]1Current NDC, 1 package rows20240816_a2a028a1-3f35-45f6-99a9-8a1c8b4c1f9b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84661-523-0084661052300177 mL in 1 CAN (84661-523-00) 177 ml2024-08-05NoNoCurrent