Dust Mix Antigen Liquid
NDC Package 43406-0140-1
Package Information
Dust Mix Antigen (antimon tart, arsenicum alb, blatta or, bromium, calc carb, cimex, drosera, hepar sulph calc, ictodes foetida, lycopodium, phos, pulsatilla, silicea terra, tabacum fumus) liquids is uSES: Temporarily relieves symptoms associated with allergic responses to dust.**. This formulation utilizes a liquid delivery system. Marketed by Natural Creations, Inc, this product is identified by NDC 43406-0140.
Identification & Billing
Clinical Specifications
- ANTIMONY POTASSIUM TARTRATE 30 [hp_C]/mL
- ARSENIC TRIOXIDE 30 [hp_C]/mL
- BLATTA ORIENTALIS 30 [hp_C]/mL
- BROMINE 30 [hp_C]/mL
- CALCIUM SULFIDE 30 [hp_C]/mL
- CIMEX LECTULARIUS 30 [hp_C]/mL
- DROSERA ROTUNDIFOLIA 30 [hp_C]/mL
- LYCOPODIUM CLAVATUM SPORE 30 [hp_C]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL
- PHOSPHORUS 30 [hp_C]/mL
- PULSATILLA VULGARIS 30 [hp_C]/mL
- SILICON DIOXIDE 30 [hp_C]/mL
- SYMPLOCARPUS FOETIDUS ROOT 30 [hp_C]/mL
- TOBACCO SMOKE 30 [hp_C]/mL
Regulatory & Marketing
Hierarchy Structure
- 43406 - Natural Creations, Inc
- 43406-0140 - Dust Mix Antigen
- 43406-0140-1 - 30 mL in 1 BOTTLE, DROPPER
- 43406-0140 - Dust Mix Antigen
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 43406-0140-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Dust Mix Antigen, a human over the counter drug labeled by Natural Creations, Inc. This liquid is formulated for oral use and contains antimony potassium tartrate; arsenic trioxide; blatta orientalis; bromine; calcium sulfide; cimex lectularius; drosera rotundifolia; lycopodium clavatum spore; oyster shell calcium carbonate, crude; phosphorus; pulsatilla vulgaris; silicon dioxide; symplocarpus foetidus root; tobacco smoke 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 Natural Creations, Inc on July 12, 2012. The current certification is valid through December 31, 2026.
How is this Natural Creations, Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43406014001. 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.