Drs. pharmacy sunscreen SPF 50

Product NDC
80489-235
11-digit product format
804890235
Labeler code
80489
Product ID
80489-235_3134c223-e293-e2e6-e063-6294a90a7cfb
Type
HUMAN OTC DRUG
Nonproprietary name
sunscreen SPF 50
Dosage form
LOTION
Route
TOPICAL
Labeler
OL PHARMA TECH LLC. (Drs. Pharmacy)
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-01-01
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 10; 5; 10 g/100g; g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Drs. pharmacy sunscreen SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTISALATE3 g/100g
HOMOSALATE10 g/100g
AVOBENZONE5 g/100g
OCTOCRYLENE10 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4X49Y0596W, V06SV4M95S, G63QQF2NOX, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80489-235-01Drs. pharmacy sunscreen SPF 50133 g in 1 TUBELOTION1333
80489-235-02Drs. pharmacy sunscreen SPF 50118 g in 1 TUBELOTION1183
80489-235-03Drs. pharmacy sunscreen SPF 5085 g in 1 TUBELOTION853

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80489-235DRS. PHARMACY SUNSCREEN SPF 50 (SUNSCREEN SPF 50) LOTION [OL PHARMA TECH LLC. (DRS. PHARMACY)]3Current NDC, 3 package rows20250330_0def5c19-b088-2ffb-e063-6394a90aa109.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80489-235-0180489023501133 g in 1 TUBE (80489-235-01) 133 g2024-01-01NoNoHistorical
80489-235-0280489023502118 g in 1 TUBE (80489-235-02) 118 g2024-01-01NoNoHistorical
80489-235-038048902350385 g in 1 TUBE (80489-235-03) 85 g2024-03-26NoNoHistorical