Cold Plus Flu Spray
NDC Package 50845-0247-1
Package Information
Cold Plus Flu (anas barbariae, hepatis et cordis extractum, antimonium tartaricum, apis mellifica, baptisia tinctoria, bryonia (alba), eupatorium perfoliatum, gelsemium sempervirens, lung suis, sambucus nigra, serum anguillae, sticta pulmonaria) sprays is adults and children over 12: Spray twice under the tongue three times per day. This formulation utilizes a spray delivery system. Marketed by Liddell Laboratories, Inc., this product is identified by NDC 50845-0247.
Identification & Billing
Clinical Specifications
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 200 [hp_C]/mL
- ANTIMONY POTASSIUM TARTRATE 200 [hp_C]/mL
- APIS MELLIFERA 200 [hp_C]/mL
- BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
- BRYONIA ALBA ROOT 200 [hp_C]/mL
- EUPATORIUM PERFOLIATUM FLOWERING TOP 200 [hp_C]/mL
- GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/mL
- SUS SCROFA LUNG 200 [hp_C]/mL
- SAMBUCUS NIGRA FLOWERING TOP 200 [hp_C]/mL
- ANGUILLA ROSTRATA BLOOD SERUM 3 [hp_X]/mL
- LOBARIA PULMONARIA 6 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 50845 - Liddell Laboratories, Inc.
- 50845-0247 - Cold Plus Flu
- 50845-0247-1 - 30 mL in 1 BOTTLE, SPRAY
- 50845-0247 - Cold Plus Flu
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 50845-0247-1 identifies a specific commercial package of 30 ml in 1 bottle, spray of Cold Plus Flu, a human over the counter drug labeled by Liddell Laboratories, Inc.. This spray is formulated for oral use and contains cairina moschata heart/liver autolysate; antimony potassium tartrate; apis mellifera; baptisia tinctoria root; bryonia alba root; eupatorium perfoliatum flowering top; gelsemium sempervirens root; sus scrofa lung; sambucus nigra flowering top; anguilla rostrata blood serum; lobaria pulmonaria 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 Liddell Laboratories, Inc. on January 15, 2019. The current certification is valid through December 31, 2026.
How is this Liddell Laboratories, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 50845024701. 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.