Home NDC 69842-123 CVS Health
Product NDC 69842-123
11-digit product format 698420123
Labeler code 69842
Product ID 69842-123_25139a12-657c-90d9-e063-6394a90acfa8
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler CVS Pharmacy
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-10-23
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 49.39; 47.145 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 CVS Health
Brand name suffix 60 Plus Sensitive Skin Sun
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 49.39 mg/mL ZINC OXIDE 47.145 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 69842-123-09 CVS Health60 Plus Sensitive Skin Sun 89 mL in 1 BOTTLE LOTION 89 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-123 CVS HEALTH 60 PLUS SENSITIVE SKIN SUN (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [CVS PHARMACY] 5 Current NDC, Legacy NDC, 1 package rows 20241024_477c25ec-33db-04a6-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 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 69842-123-09 69842012309 89 mL in 1 BOTTLE (69842-123-09) 89 ml 2015-10-23 0000-00-00 No No Current