Rehydrate Liquid
NDC Package 54638-0003-1
Package Information
Rehydrate (avena sativa, equisetum hyemale, hypericum perforatum, ulmus fulva, glycyrrhiza glabra, silicea, pueraria lobata, carlsbad aqua, adenosinum triphosphoricum dinatrum, germanium sesquioxide, hydrogen, oxygen, wiesbaden) liquids is to aid with proper hydration. This formulation utilizes a liquid delivery system. Marketed by Paradocs All Natural, Inc., this product is identified by NDC 54638-0003.
Identification & Billing
Clinical Specifications
- AVENA SATIVA FLOWERING TOP 30 [hp_C]/mL
- EQUISETUM HYEMALE 3 [hp_X]/mL
- HYPERICUM PERFORATUM 4 [hp_X]/mL
- ULMUS RUBRA BARK 30 [hp_C]/mL
- GLYCYRRHIZA GLABRA 12 [hp_X]/mL
- SILICON DIOXIDE 30 [hp_C]/mL
- PUERARIA MONTANA VAR. LOBATA ROOT 6 [hp_X]/mL
- WATER 30 [hp_C]/mL
- ADENOSINE TRIPHOSPHATE DISODIUM 8 [hp_C]/mL
- GERMANIUM SESQUIOXIDE 12 [hp_X]/mL
- HYDROGEN 6 [hp_X]/mL
- OXYGEN 12 [hp_C]/mL
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 54638 - Paradocs All Natural, Inc.
- 54638-0003 - Rehydrate
- 54638-0003-1 - 60 mL in 1 BOTTLE, DROPPER
- 54638-0003 - Rehydrate
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 54638-0003-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Rehydrate, a human over the counter drug labeled by Paradocs All Natural, Inc.. This liquid is formulated for oral use and contains avena sativa flowering top; equisetum hyemale; hypericum perforatum; ulmus rubra bark; glycyrrhiza glabra; silicon dioxide; pueraria montana var. lobata root; water; adenosine triphosphate disodium; germanium sesquioxide; hydrogen; oxygen 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 Paradocs All Natural, Inc. on February 12, 2015. The current certification is valid through December 31, 2026.
How is this Paradocs All Natural, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 54638000301. 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.