Marlowe

Product NDC
82215-0001
11-digit product format
822150001
Labeler code
82215
Product ID
82215-0001_2526d928-68d0-b159-e063-6294a90ae78f
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
Marlowe Holdings, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-04-14
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
29.94; 99.8; 49.9; 49.9 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
Marlowe
Brand name suffix
SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE29.94 mg/mL
HOMOSALATE99.8 mg/mL
OCTISALATE49.9 mg/mL
OCTOCRYLENE49.9 mg/mL

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82215-0001-3MarloweSPF 50100 mL in 1 TUBELOTION1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82215-0001MARLOWE SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [MARLOWE HOLDINGS, LLC]3Current NDC, 1 package rows20241025_f94bd91a-f0ab-680c-e053-6394a90ac855.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82215-0001-382215000103100 mL in 1 TUBE (82215-0001-3) 100 ml2023-04-14NoNoHistorical