Home NDC 69949-010 NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER
Product NDC 69949-010
11-digit product format 699490010
Labeler code 69949
Product ID 69949-010_3dc666fa-dd86-4924-9b90-50d240203981
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler Synchronicity Spa, Inc. DBA Suntegrity
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-08-12
Substance ZINC OXIDE
Active strength 200 mg/g
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 NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 200 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69949-010-01 NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER 50 g in 1 CANISTER CREAM 50 2 69949-010-02 NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER 50 g in 1 BOX CREAM 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69949-010 NATURAL MOISTURIZING FACE SUNSCREEN AND PRIMER (ZINC OXIDE) CREAM [SYNCHRONICITY SPA, INC. DBA SUNTEGRITY] 2 Current NDC, Legacy NDC, 2 package rows 20241124_5996f9b2-18c1-4c8f-a0ab-eca180db61ad.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 69949-010-01 69949001001 50 g in 1 CANISTER (69949-010-01) 50 g 2010-08-12 0000-00-00 No No Current 69949-010-02 69949001002 50 g in 1 BOX (69949-010-02) 50 g 2020-07-01 0000-00-00 No No Current