Home NDC 80325-001 Spit and Polish Sun Smart Sunscreen
Product NDC 80325-001
11-digit product format 803250001
Labeler code 80325
Product ID 80325-001_09c2d4fa-e9fb-318b-e063-6394a90a6d51
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE, ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler Naturally Uncommon, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-03-01
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 70; 100 mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 Spit and Polish Sun Smart Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 70 mg/mL ZINC OXIDE 100 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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 80325-001-01 Spit and Polish Sun Smart Sunscreen 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 80325-001 SPIT AND POLISH SUN SMART SUNSCREEN (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [NATURALLY UNCOMMON, LLC] 2 Current NDC, Legacy NDC, 1 package rows 20231110_af879a05-1483-5c11-e053-2995a90af45d.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 27 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 80325-001-01 80325000101 177 mL in 1 TUBE (80325-001-01) 177 ml 2020-03-01 0000-00-00 No No Current