Home NDC 69968-0799 Johnson and Johnson First Aid Travel Ready
Product NDC 69968-0799
11-digit product format 699680799
Labeler code 69968
Product ID 69968-0799_4248165f-8b3b-312f-e063-6394a90a696c
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Neomycin Sulfate, Polymyxin B Sulfate, Pramoxine Hydrochloride
Dosage form KIT
Labeler Kenvue Brands LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-01-31
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 Johnson and Johnson First Aid Travel Ready
Brand name suffix 80 CT
Listing expiration 2026-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198440 Internal RxNorm lookup 209459 Internal RxNorm lookup 1359360 Internal RxNorm 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 50580-449-08 Johnson and Johnson First Aid Travel Ready80 CT 2 in 1 POUCH TABLET, FILM COATED 4 500 mg 3 69968-0055-2 Johnson and Johnson First Aid Travel Ready80 CT 14.2 g in 1 TUBE CREAM 14.2 g 10 mg in 1g 3 69968-0055-2 Johnson and Johnson First Aid Travel Ready80 CT 1 in 1 CARTON CREAM 10 mg in 1g 3 69968-0799-9 Johnson and Johnson First Aid Travel Ready80 CT 1 in 1 PACKAGE KIT 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0799 JOHNSON AND JOHNSON FIRST AID TRAVEL READY 80 CT (ACETAMINOPHEN, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE) KIT [KENVUE BRANDS LLC] 2 Current NDC, 4 package rows 20241116_f388f105-48ba-4616-e053-2a95a90a0049.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 116 of 152 · 3,029 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 50580-449-08 50580044908 2 in 1 POUCH Historical 69968-0055-2 69968005502 14.2 g in 1 TUBE 14.2 g Historical 69968-0799-9 69968079909 1 KIT in 1 PACKAGE (69968-0799-9) * 1 TUBE in 1 CARTON (69968-0055-2) / 14.2 g in 1 TUBE * 1 CLOTH in 1 PACKET * 2 TABLET, FILM COATED in 1 POUCH (50580-449-08) 1 kit 2022-01-31 No No Current