Home NDC 69949-025 Mineral Sun Drops
Product NDC 69949-025
11-digit product format 699490025
Labeler code 69949
Product ID 69949-025_1461504e-866d-44d4-a4d9-60b2ba8ce33e
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Synchronicity Spa, Inc. DBA Suntegrity
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-15
Substance ZINC OXIDE
Active strength 220 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 Mineral Sun Drops
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 220 mg/mL
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 69949-025-01 Mineral Sun Drops 30 mL in 1 BOTTLE, DROPPER LOTION 30 1 69949-025-01 Mineral Sun Drops 1 in 1 BOX LOTION 1 1
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 Marketing start Sample Exclude flag Status 69949-025-01 69949002501 1 BOTTLE, DROPPER in 1 BOX (69949-025-01) / 30 mL in 1 BOTTLE, DROPPER 2025-08-15 No No Current