Ohm-inma Spray
NDC Package 66096-757-02
Package Information
Ohm-inma (aconitum napellus, aranea diadema, arnica montana, asclepias vincetoxicum, baptisia tinctoria, bryonia alba, echinacea angustifolia, equisetum hyemale, eupatorium perforliatum, gelsemium sempervirens, hepar sulphuris calcareum, juglans regia, phytolacca decandra, sanguinaria canadensis, sarsaparilla, sulphur, zincum metallicum) sprays is a human prescription drug administered via oral route. This formulation utilizes a spray delivery system. Marketed by Ohm Pharma Inc., this product is identified by NDC 66096-757.
Identification & Billing
Clinical Specifications
- ACONITUM NAPELLUS 7 [hp_X]/30mL
- ARANEUS DIADEMATUS 9 [hp_X]/30mL
- ARNICA MONTANA 6 [hp_X]/30mL
- BAPTISIA TINCTORIA 8 [hp_X]/30mL
- BRYONIA ALBA ROOT 10 [hp_X]/30mL
- CALCIUM SULFIDE 12 [hp_X]/30mL
- CYNANCHUM VINCETOXICUM ROOT 12 [hp_X]/30mL
- ECHINACEA ANGUSTIFOLIA 6 [hp_X]/30mL
- EQUISETUM HYEMALE 7 [hp_X]/30mL
- EUPATORIUM PERFOLIATUM FLOWERING TOP 10 [hp_X]/30mL
- GELSEMIUM SEMPERVIRENS ROOT 8 [hp_X]/30mL
- JUGLANS REGIA LEAF 6 [hp_X]/30mL
- PHYTOLACCA AMERICANA ROOT 10 [hp_X]/30mL
- SANGUINARIA CANADENSIS ROOT 8 [hp_X]/30mL
- SARSAPARILLA 9 [hp_X]/30mL
- SULFUR 10 [hp_X]/30mL
- ZINC 12 [hp_X]/30mL
Regulatory & Marketing
Hierarchy Structure
- 66096 - Ohm Pharma Inc.
- 66096-757 - Ohm-inma
- 66096-757-02 - 30 mL in 1 BOTTLE, SPRAY
- 66096-757 - Ohm-inma
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 66096-757-02 identifies a specific commercial package of 30 ml in 1 bottle, spray of Ohm-inma, a human prescription drug labeled by Ohm Pharma Inc.. This spray is formulated for oral use and contains aconitum napellus; araneus diadematus; arnica montana; baptisia tinctoria; bryonia alba root; calcium sulfide; cynanchum vincetoxicum root; echinacea angustifolia; equisetum hyemale; eupatorium perfoliatum flowering top; gelsemium sempervirens root; juglans regia leaf; phytolacca americana root; sanguinaria canadensis root; sarsaparilla; sulfur; zinc 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 Ohm Pharma Inc. on December 19, 2018. The current certification is valid through December 31, 2026.
How is this Ohm Pharma Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 66096075702. 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 Product segment to maintain the 5-4-2 structure.