Ed Bron Gp Liquid
NDC Package 0485-0208-16
Package Information
Ed Bron Gp (guaifenesin and phenylephrine) liquids is do not exceed recommended dosage.Adults and children 12 years of age and over:2 teaspoonfuls (10 mL) every 4 hours, not to exceed 12 teaspoonfuls in 24 hours, or as directed by a doctor.Children 6 to under 12 years of age:1 teaspoonful (5 mL) every 4 hours, not to exceed 6 teaspoonfuls in 24 hours, or as directed by a doctor.Children under 6 years of age:Consult a doctor. This formulation utilizes a liquid delivery system. Marketed by Edwards Pharmaceuticals, Inc., this product is identified by NDC 0485-0208.
Identification & Billing
- RxCUI: 1358627 - guaiFENesin 100 MG / phenylephrine HCl 5 MG in 5 mL Oral Solution
- RxCUI: 1358627 - guaifenesin 20 MG/ML / phenylephrine hydrochloride 1 MG/ML Oral Solution
- RxCUI: 1358627 - guaifenesin 100 MG / phenylephrine hydrochloride 5 MG per 5 ML Oral Solution
Clinical Specifications
- Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
- Decreased Respiratory Secretion Viscosity - [PE] (Physiologic Effect)
- Expectorant - [EPC] (Established Pharmacologic Class)
- Increased Respiratory Secretions - [PE] (Physiologic Effect)
- alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 0485 - Edwards Pharmaceuticals, Inc.
- 0485-0208 - Ed Bron Gp
- 0485-0208-16 - 473 mL in 1 BOTTLE, PLASTIC
- 0485-0208 - Ed Bron Gp
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 0485-0208-16 identifies a specific commercial package of 473 ml in 1 bottle, plastic of Ed Bron Gp, a human over the counter drug labeled by Edwards Pharmaceuticals, Inc.. This product is billed per "ML" milliliter and contains an estimated amount of 473 billable units per package. This liquid is formulated for oral use and contains guaifenesin; phenylephrine hydrochloride 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 Edwards Pharmaceuticals, Inc. on June 01, 2012. The current certification is valid through December 31, 2026.
How is this Edwards Pharmaceuticals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00485020816. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 473 total billable units per package. 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 Labeler segment to maintain the 5-4-2 structure.