Equate

Product NDC
49035-759
11-digit product format
490350759
Labeler code
49035
Product ID
49035-759_249e9a6e-b52d-0c56-e063-6394a90a6664
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
Wal-Mart Stores Inc
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-06-04
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 150; 50; 70 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
Equate
Brand name suffix
SPF 50 Ultra Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE150 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE70 mg/mL

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-759-12EquateSPF 50 Ultra Sunscreen236 mL in 1 TUBELOTION2365
49035-759-14EquateSPF 50 Ultra Sunscreen473 mL in 1 BOTTLE, PLASTICLOTION4735

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-759EQUATE SPF 50 ULTRA SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [WAL-MART STORES INC]5Current NDC, Legacy NDC, 2 package rows20241018_8f02f297-5315-ced4-e053-2a95a90a8c7b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49035-759-1249035075912236 mL in 1 TUBE (49035-759-12) 236 ml2019-06-040000-00-00NoNoCurrent
49035-759-1449035075914473 mL in 1 BOTTLE, PLASTIC (49035-759-14) 473 ml2019-06-040000-00-00NoNoCurrent