Itch Formula Liquid
NDC Package 43742-2219-1
Package Information
Itch Formula (antipyrinum, apis mellifica, calendula officinalis, cantharis, copaiva officinalis, croton tiglium, graphites, histaminum hydrochloricum, ledum palustre, mezereum, natrum muriaticum, petroleum, rhus venenata, staphysagria, sulphur, urtica urens) liquids is 1-10 drops under the tongue, 3 times a day or as directed by a health professional. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-2219.
Identification & Billing
Clinical Specifications
- ANTIPYRINE 18 [hp_X]/mL
- APIS MELLIFERA 6 [hp_X]/mL
- CALENDULA OFFICINALIS FLOWERING TOP 3 [hp_X]/mL
- COPAIFERA OFFICINALIS RESIN 10 [hp_X]/mL
- CROTON TIGLIUM SEED 12 [hp_X]/mL
- DAPHNE MEZEREUM BARK 12 [hp_X]/mL
- DELPHINIUM STAPHISAGRIA SEED 12 [hp_X]/mL
- GRAPHITE 12 [hp_Q]/mL
- HISTAMINE DIHYDROCHLORIDE 6 [hp_X]/mL
- KEROSENE 12 [hp_X]/mL
- LYTTA VESICATORIA 12 [hp_X]/mL
- RHODODENDRON TOMENTOSUM LEAFY TWIG 6 [hp_X]/mL
- SODIUM CHLORIDE 6 [hp_X]/mL
- SULFUR 8 [hp_X]/mL
- TOXICODENDRON VERNIX LEAFY TWIG 12 [hp_X]/mL
- URTICA URENS WHOLE 6 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc.
- 43742-2219 - Itch Formula
- 43742-2219-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-2219 - Itch Formula
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 43742-2219-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Itch Formula, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains antipyrine; apis mellifera; calendula officinalis flowering top; copaifera officinalis resin; croton tiglium seed; daphne mezereum bark; delphinium staphisagria seed; graphite; histamine dihydrochloride; kerosene; lytta vesicatoria; rhododendron tomentosum leafy twig; sodium chloride; sulfur; toxicodendron vernix leafy twig; urtica urens whole 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 Deseret Biologicals, Inc. on November 12, 2024. The current certification is valid through December 31, 2026.
How is this Deseret Biologicals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742221901. 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.