Home NDC 49035-759 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 HOMOSALATE; AVOBENZONE; OCTISALATE; OCTOCRYLENE
Active strength 150; 30; 50; 70 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Equate
Brand name suffix SPF 50 Ultra Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 150 mg/mL AVOBENZONE 30 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 70 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49035-759-12 EquateSPF 50 Ultra Sunscreen 236 mL in 1 TUBE LOTION 236 5 49035-759-14 EquateSPF 50 Ultra Sunscreen 473 mL in 1 BOTTLE, PLASTIC LOTION 473 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49035-759 EQUATE SPF 50 ULTRA SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [WAL-MART STORES INC] 5 Current NDC, Legacy NDC, 2 package rows 20241018_8f02f297-5315-ced4-e053-2a95a90a8c7b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49035-759-12 49035075912 236 mL in 1 TUBE (49035-759-12) 236 ml 2019-06-04 0000-00-00 No No Current 49035-759-14 49035075914 473 mL in 1 BOTTLE, PLASTIC (49035-759-14) 473 ml 2019-06-04 0000-00-00 No No Current