Home NDC 10967-652 Revlon Colorstay Preo and Protect Primer
Product NDC 10967-652
11-digit product format 109670652
Labeler code 10967
Product ID 10967-652_2a9692e8-80b4-15a8-e063-6394a90aa10d
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide, Octinoxate Primer
Dosage form LIQUID
Route TOPICAL
Labeler Revlon Consumer Products Corp
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-01-01
Substance ZINC OXIDE; OCTINOXATE; TITANIUM DIOXIDE
Active strength 9; 7.5; 3.6 mg/mL; 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 Revlon Colorstay Preo and Protect Primer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 9 mg/mL OCTINOXATE 7.5 mg/mL TITANIUM DIOXIDE 3.6 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup 15FIX9V2JP 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 10967-652-11 Revlon Colorstay Preo and Protect Primer 26.6 mL in 1 BOTTLE, PLASTIC LIQUID 26.6 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10967-652 REVLON COLORSTAY PREO AND PROTECT PRIMER (TITANIUM DIOXIDE, ZINC OXIDE, OCTINOXATE PRIMER) LIQUID [REVLON CONSUMER PRODUCTS CORP] 2 Current NDC, Legacy NDC, 1 package rows 20250101_8eebf23e-7fce-dfc0-e053-2995a90ae322.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 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 10967-652-11 10967065211 26.6 mL in 1 BOTTLE, PLASTIC (10967-652-11) 26.6 ml 2019-01-01 0000-00-00 No No Current