Cosmestat Liquid
NDC Package 44911-0671-1
Package Information
Cosmestat (alfalfa, avena sativa, iodium, bovista, formalinum, hypophysis suis, manganum aceticum, natrum muriaticum, petroleum, pulsatilla (pratensis), rhus tox, terebinthina, thyroidinum (bovine), cortisone aceticum) liquids is adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0671.
Identification & Billing
Clinical Specifications
- AVENA SATIVA FLOWERING TOP 3 [hp_X]/mL
- CORTISONE ACETATE 30 [hp_X]/mL
- FORMALDEHYDE SOLUTION 12 [hp_X]/mL
- IODINE 6 [hp_X]/mL
- KEROSENE 12 [hp_X]/mL
- LYCOPERDON UTRIFORME FRUITING BODY 12 [hp_X]/mL
- MANGANESE ACETATE TETRAHYDRATE 12 [hp_X]/mL
- MEDICAGO SATIVA WHOLE 3 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 12 [hp_X]/mL
- SODIUM CHLORIDE 12 [hp_X]/mL
- SUS SCROFA PITUITARY GLAND 12 [hp_X]/mL
- THYROID, BOVINE 12 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
- TURPENTINE OIL 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0671 - Cosmestat
- 44911-0671-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0671 - Cosmestat
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 44911-0671-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Cosmestat, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains avena sativa flowering top; cortisone acetate; formaldehyde solution; iodine; kerosene; lycoperdon utriforme fruiting body; manganese acetate tetrahydrate; medicago sativa whole; pulsatilla pratensis whole; sodium chloride; sus scrofa pituitary gland; thyroid, bovine; toxicodendron pubescens leaf; turpentine oil 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 Energique, Inc. on April 17, 2023. The current certification is valid through December 31, 2026.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911067101. 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.