Home NDC 59427-113 DR ANDREW WEILS FOR ORIGINS
Product NDC 59427-113
11-digit product format 594270113
Labeler code 59427
Product ID 59427-113_051acbc2-7bef-4059-e063-6394a90a115b
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE and ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler ORIGINS NATURAL RESOURCES INC.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-02-15
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 63; 40 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 DR ANDREW WEILS FOR ORIGINS
Brand name suffix MEGA-DEFENSE ADVANCED DAILY UV DEFENDER BROAD SPECTRUM SPF 45
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 63 mg/mL ZINC OXIDE 40 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59427-113-01 DR ANDREW WEILS FOR ORIGINSMEGA-DEFENSE ADVANCED DAILY UV DEFENDER BROAD SPECTRUM SPF 45 1 in 1 CARTON LOTION 1 7 59427-113-01 DR ANDREW WEILS FOR ORIGINSMEGA-DEFENSE ADVANCED DAILY UV DEFENDER BROAD SPECTRUM SPF 45 30 mL in 1 BOTTLE LOTION 30 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59427-113 DR ANDREW WEILS FOR ORIGINS MEGA-DEFENSE ADVANCED DAILY UV DEFENDER BROAD SPECTRUM SPF 45 (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [ORIGINS NATURAL RESOURCES INC.] 7 Current NDC, Legacy NDC, 2 package rows 20231020_11248cab-c3a5-4e16-8280-9f70bb863cf7.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 81 of 354 · 7,077 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 59427-113-01 59427011301 1 BOTTLE in 1 CARTON (59427-113-01) / 30 mL in 1 BOTTLE 1 bottle 2016-02-15 0000-00-00 No No Current