Home NDC 73670-609 NAELI Tinted Mineral Moisturizer Sunscreen SPF 50, Light
Product NDC 73670-609
11-digit product format 736700609
Labeler code 73670
Product ID 73670-609_35b66420-ac52-494b-e063-6294a90a5955
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form LIQUID
Route TOPICAL
Labeler ALLI LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-04
Substance ZINC OXIDE
Active strength 180 mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 NAELI Tinted Mineral Moisturizer Sunscreen SPF 50, Light
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 180 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73670-609-00 NAELI Tinted Mineral Moisturizer Sunscreen SPF 50, Light 1 in 1 BOX LIQUID 1 1 73670-609-00 NAELI Tinted Mineral Moisturizer Sunscreen SPF 50, Light 41.4 mL in 1 BOTTLE LIQUID 41.4 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73670-609 NAELI TINTED MINERAL MOISTURIZER SUNSCREEN SPF 50, LIGHT (ZINC OXIDE) LIQUID [ALLI LLC] 1 Current NDC, 2 package rows 20250523_3cb4459b-1776-414a-b5c4-0ffb9f1df766.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 Sample Exclude flag Status 73670-609-00 73670060900 1 BOTTLE in 1 BOX (73670-609-00) / 41.4 mL in 1 BOTTLE 1 bottle 2025-04-04 No No Current