NDC Package 0067-0100-99 Theraflu Severe Cold Relief Daytime

Acetaminophen,Dextromethorphan Hbr Powder, For Solution Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0067-0100-99
Package Description:
1000 PACKET in 1 CONTAINER / 1 POWDER, FOR SOLUTION in 1 PACKET
Product Code:
Proprietary Name:
Theraflu Severe Cold Relief Daytime
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hbr
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide
Usage Information:
Do not use more than directedtake every 4 hours, while symptoms persist. Do not take more than 6 packets in 24 hours unless directed by a doctor.AgeDoseadults and children12 years of age and overone packetchildren under12 years of agedo not usedissolve contents of one packet into 8 oz. hot water; sip while hot. Consume entire drink within 10-15 minutes.if using a microwave, add contents of one packet to 8 oz. of cool water; stir briskly before and after heating. Do not overheat.
11-Digit NDC Billing Format:
00067010099
NDC to RxNorm Crosswalk:
  • RxCUI: 2670598 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG Powder for Oral Solution
  • RxCUI: 2670598 - APAP 500 MG / dextromethorphan hydrobromide 20 MG Powder for Oral Solution
Product Type:
Human Otc Drug
Labeler Name:
Haleon Us Holdings Llc
Dosage Form:
Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
12-01-2023
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0067-0100-066 PACKET in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 PACKET

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Frequently Asked Questions

What is NDC 0067-0100-99?

The NDC Packaged Code 0067-0100-99 is assigned to a package of 1000 packet in 1 container / 1 powder, for solution in 1 packet of Theraflu Severe Cold Relief Daytime, a human over the counter drug labeled by Haleon Us Holdings Llc. The product's dosage form is powder, for solution and is administered via oral form.

Is NDC 0067-0100 included in the NDC Directory?

Yes, Theraflu Severe Cold Relief Daytime with product code 0067-0100 is active and included in the NDC Directory. The product was first marketed by Haleon Us Holdings Llc on December 01, 2023 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0067-0100-99?

The 11-digit format is 00067010099. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
4-4-20067-0100-995-4-200067-0100-99