Home NDC 49527-074-01 MOISTURE SURGE SHEERTINT HYDRATOR BROAD SPECTRUM SPF 25
Product NDC 49527-074
Requested package NDC 49527-074-01
11-digit product format 495270074
Labeler code 49527
Product ID 49527-074_079c68e7-7fd2-9bb9-e063-6394a90a5f8e
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, and ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler CLINIQUE LABORATORIES LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-10-16
Substance OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength 75; 45; 38; 36 mg/mL; 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 MOISTURE SURGE SHEERTINT HYDRATOR BROAD SPECTRUM SPF 25
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 75 mg/mL OCTISALATE 45 mg/mL TITANIUM DIOXIDE 38 mg/mL ZINC OXIDE 36 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49527-074-01 MOISTURE SURGE SHEERTINT HYDRATOR BROAD SPECTRUM SPF 25 40 mL in 1 TUBE CREAM 40 7 49527-074-01 MOISTURE SURGE SHEERTINT HYDRATOR BROAD SPECTRUM SPF 25 1 in 1 CARTON CREAM 1 7 49527-074-02 MOISTURE SURGE SHEERTINT HYDRATOR BROAD SPECTRUM SPF 25 1 mL in 1 TUBE CREAM 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49527-074 MOISTURE SURGE SHEERTINT HYDRATOR BROAD SPECTRUM SPF 25 (OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, AND ZINC OXIDE) CREAM [CLINIQUE LABORATORIES LLC] 7 Current NDC, Legacy NDC, 3 package rows 20231019_159410d4-4479-4442-b371-bde72aae3e1e.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 49527-074-01 49527007401 1 TUBE in 1 CARTON (49527-074-01) / 40 mL in 1 TUBE 1 tube 2019-10-16 0000-00-00 No No Current