Poolside Sun Daze Body Illuminator SPF 30 Shimmer Sunscreen

Product NDC
85179-042
11-digit product format
851790042
Labeler code
85179
Product ID
85179-042_495fecfb-ffc3-e7bb-e063-6294a90a1308
Type
HUMAN OTC DRUG
Nonproprietary name
HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Dosage form
GEL
Route
TOPICAL
Labeler
I World LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-12-17
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 100; 50; 60 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Poolside Sun Daze Body Illuminator SPF 30 Shimmer Sunscreen
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE100 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE60 mg/mL

Harmonized Identifiers#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85179-042-00Poolside Sun Daze Body Illuminator SPF 30 Shimmer Sunscreen100 mL in 1 BOTTLEGEL1001

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85179-042-0085179004200100 mL in 1 BOTTLE (85179-042-00) 100 ml2025-12-17NoNoCurrent