JESS BEAUTY Let It Sun Sunscreen SPF-50

Product NDC
83542-410
11-digit product format
835420410
Labeler code
83542
Product ID
83542-410_09764ab9-1a62-b42b-e063-6394a90a4a77
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form
LOTION
Route
TOPICAL
Labeler
JESS BEAUTY PRODUCTS LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-06-30
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 100; 50; 100 mg/mL; 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
JESS BEAUTY Let It Sun Sunscreen SPF-50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE100 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE100 mg/mL

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83542-410-00JESS BEAUTY Let It Sun Sunscreen SPF-5050 mL in 1 TUBELOTION502
83542-410-00JESS BEAUTY Let It Sun Sunscreen SPF-501 in 1 BOXLOTION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83542-410JESS BEAUTY LET IT SUN SUNSCREEN SPF-50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [JESS BEAUTY PRODUCTS LLC]2Current NDC, 2 package rows20231106_88628c11-dbc7-4404-9701-7944a685a13d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83542-410-00835420410001 TUBE in 1 BOX (83542-410-00) / 50 mL in 1 TUBE1 tube2023-06-30NoNoHistorical