Home NDC 83108-210 Rationale The Discovery Travel Kit
Product NDC 83108-210
11-digit product format 831080210
Labeler code 83108
Product ID 83108-210_4b17263c-0cff-6d15-e063-6394a90a391b
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form KIT
Labeler RATIONALE GROUP PTY LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-17
NDC exclude flag No
Listing certified through 2027-12-31
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 Rationale The Discovery Travel Kit
Listing expiration 2027-12-31 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 83108-210-00 Rationale The Discovery Travel Kit 1 in 1 KIT KIT 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 Units Marketing start Sample Exclude flag Status 83108-210-00 83108021000 1 KIT in 1 KIT (83108-210-00) * 1 BOTTLE, PLASTIC in 1 CARTON (83108-200-15) / 15 mL in 1 BOTTLE, PLASTIC 1 kit 2026-02-17 No No Current