Home NDC 79903-019 WALMART EQUATE BEAUTY ULTRA LIGHT SUNSCREEN SPF 100
Product NDC 79903-019
11-digit product format 799030019
Labeler code 79903
Product ID 79903-019_252886c8-ae3f-0f06-e063-6294a90a5949
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Dosage form LOTION
Route TOPICAL
Labeler WAL-MART STORES INC.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-10-08
Substance AVOBENZONE; HOMOSALATE; OXYBENZONE; OCTOCRYLENE; OCTISALATE
Active strength 30; 150; 60; 100; 50 mg/mL; 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 WALMART EQUATE BEAUTY ULTRA LIGHT SUNSCREEN SPF 100
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 150 mg/mL OXYBENZONE 60 mg/mL OCTOCRYLENE 100 mg/mL OCTISALATE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79903-019-15 WALMART EQUATE BEAUTY ULTRA LIGHT SUNSCREEN SPF 100 177 mL in 1 TUBE LOTION 177 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79903-019 WALMART EQUATE BEAUTY ULTRA LIGHT SUNSCREEN SPF 100 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [WAL-MART STORES INC.] 2 Current NDC, Legacy NDC, 1 package rows 20241025_c8d4feca-7bee-2413-e053-2a95a90a739c.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 242 of 353 · 7,041 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 79903-019-15 79903001915 177 mL in 1 TUBE (79903-019-15) 177 ml 2020-10-08 0000-00-00 No No Current