Home NDC 46783-222 Reactive Plus Anti-Oxidant Serum plus Broad-spectrum SPF 45
Product NDC 46783-222
11-digit product format 467830222
Labeler code 46783
Product ID 46783-222_1aeba243-558e-442e-ad8a-0f96a0940583
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate and Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Merz North America, Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-06-01
Substance OCTINOXATE; ZINC OXIDE
Active strength 50; 51 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 Reactive Plus Anti-Oxidant Serum plus Broad-spectrum SPF 45
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 50 mg/mL ZINC OXIDE 51 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 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 46783-222-04 Reactive Plus Anti-Oxidant Serum plus Broad-spectrum SPF 45 4 mL in 1 TUBE LOTION 4 8 46783-222-30 Reactive Plus Anti-Oxidant Serum plus Broad-spectrum SPF 45 30 mL in 1 BOTTLE LOTION 30 8 46783-222-30 Reactive Plus Anti-Oxidant Serum plus Broad-spectrum SPF 45 1 in 1 CARTON LOTION 1 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 46783-222 REACTIVE PLUS ANTI-OXIDANT SERUM PLUS BROAD-SPECTRUM SPF 45 (OCTINOXATE AND ZINC OXIDE) LOTION [MERZ NORTH AMERICA, INC] 7 Current NDC, Legacy NDC, 3 package rows 20241109_62c822d9-c8ed-4b95-8d88-806295f5a936.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 46783-222-04 46783022204 4 mL in 1 TUBE (46783-222-04) 4 ml 2019-06-15 0000-00-00 Yes No Current 46783-222-30 46783022230 1 BOTTLE in 1 CARTON (46783-222-30) / 30 mL in 1 BOTTLE 1 bottle 2018-06-01 0000-00-00 No No Current