Home NDC 68062-8307 Natural SPF 50
Product NDC 68062-8307
11-digit product format 680628307
Labeler code 68062
Product ID 68062-8307_5b8dd5df-084e-2ba7-e063-6394a90aaeac
Type HUMAN OTC DRUG
Nonproprietary name titanium dioxide, zinc oxide
Dosage form LOTION
Route TOPICAL
Labeler Spa de Soleil
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-05-04
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 780; 900 mg/118mL; mg/118mL
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 Natural SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 780 mg/118mL ZINC OXIDE 900 mg/118mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68062-8307-1 Natural SPF 50 118 mL in 1 BOTTLE, PUMP LOTION 118 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68062-8307 NATURAL SPF 50 (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [SPA DE SOLEIL] 6 Current NDC, Legacy NDC, 1 package rows 20250104_4eb87d1e-601a-1209-e054-00144ff8d46c.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 68062-8307-1 68062830701 118 mL in 1 BOTTLE, PUMP (68062-8307-1) 118 ml 2017-05-04 0000-00-00 No No Current