La Roche Posay Anthelios Sunscreen SPF 60 Ultra light

Product NDC
82046-692
11-digit product format
820460692
Labeler code
82046
Product ID
82046-692_b53a13e6-4730-4d15-8991-482725bbbca0
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Dosage form
SPRAY
Route
TOPICAL
Labeler
L'Oreal USA, Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2014-01-01
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength
27; 96; 29; 54; 35 mg/g; mg/g; mg/g; mg/g; mg/g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
La Roche Posay Anthelios Sunscreen SPF 60 Ultra light
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE27 mg/g
HOMOSALATE96 mg/g
OCTISALATE29 mg/g
OCTOCRYLENE54 mg/g
OXYBENZONE35 mg/g

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82046-692-01La Roche Posay Anthelios Sunscreen SPF 60 Ultra light143 g in 1 CANSPRAY1433

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82046-692LA ROCHE POSAY ANTHELIOS SUNSCREEN SPF 60 ULTRA LIGHT (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [L'OREAL USA, INC.]2Current NDC, Legacy NDC, 1 package rows20231222_dad00eee-92cd-7610-e053-2a95a90a1fac.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82046-692-0182046069201143 g in 1 CAN (82046-692-01) 143 g2014-01-010000-00-00NoNoCurrent