Johnson And Johnson First Aid Travel Ready Kit
NDC Package 69968-0799-9
Package Information
Johnson And Johnson First Aid Travel Ready (acetaminophen, neomycin sulfate, polymyxin b sulfate, pramoxine hydrochloride) kits is do not take more than directed (see overdose warning)adults and children 12 years and overtake 2 caplets every 6 hours while symptoms lastdo not take more than 6 caplets in 24 hours, unless directed by a doctordo not use for more than 10 days unless directed by a doctorchildren under 12 yearsask a doctor adults and children 2 years of age and older: clean the affected areaapply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times dailymay be covered with a sterile bandagechildren under 2 years of age: ask a doctor. This formulation utilizes a kit delivery system. Marketed by Kenvue Brands Llc, this product is identified by NDC 69968-0799 and is authorized under FDA application M017.
Identification & Billing
- RxCUI: 1359360 - neomycin 3.5 MG / polymyxin B 10,000 UNT / pramoxine HCl 10 MG per GM Topical Cream
- RxCUI: 1359360 - neomycin 3.5 MG/ML / polymyxin B 10000 UNT/ML / pramoxine hydrochloride 10 MG/ML Topical Cream
- RxCUI: 1359360 - neomycin (as neomycin sulfate) 0.35 % / polymyxin B (as polymyxin B sulfate) 10,000 UNT/ML / pramoxine (as pramoxine HCl) 1 % Topical Cream
- RxCUI: 1359360 - neomycin 0.35 % / polymyxin B 10,000 UNT/ML / pramoxine HCl 1 % Topical Cream
- RxCUI: 198440 - acetaminophen 500 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 69968 - Kenvue Brands Llc
- 69968-0799 - Johnson And Johnson First Aid Travel Ready
- 69968-0799-9 - 1 KIT in 1 PACKAGE * 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)
- 69968-0799 - Johnson And Johnson First Aid Travel Ready
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 69968-0799-9 identifies a specific commercial package of 1 kit in 1 package * 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) of Johnson And Johnson First Aid Travel Ready 80 Ct, a human over the counter drug labeled by Kenvue Brands Llc. This kit is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Kenvue Brands Llc on January 31, 2022. The current certification is valid through December 31, 2026.
How is this Kenvue Brands Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69968079909. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.
