FDA.reportPublic FDA data

Aldi Lacura Ultra Light Body SPF 100

Product NDC
64024-945
11-digit product format
640240945
Labeler code
64024
Product ID
64024-945_25038117-204e-80a5-e063-6394a90a8ce8
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Dosage form
SPRAY
Route
TOPICAL
Labeler
ALDI INC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-01-24
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength
30; 150; 50; 100; 60 mg/g; mg/g; mg/g; mg/g; mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Aldi Lacura Ultra Light Body SPF 100
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/g
HOMOSALATE150 mg/g
OCTISALATE50 mg/g
OCTOCRYLENE100 mg/g
OXYBENZONE60 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM, 95OOS7VE0Y

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64024-945-35Aldi Lacura Ultra Light Body SPF 100142 g in 1 CANSPRAY1422

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64024-945ALDI LACURA ULTRA LIGHT BODY SPF 100 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALDI INC]2Current NDC, 1 package rows20241023_f7ac082c-def8-4379-e053-6294a90a57e3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
64024-945-3564024094535142 g in 1 CAN (64024-945-35) 142 g2022-01-24NoNoHistorical