Children Coldcalm Pellet
NDC Package 0220-9049-42
Package Information
Children Coldcalm (onion, apis mellifera, atropa belladonna, eupatorium perfoliatum flowering top, gelsemium sempervirens root, potassium dichromate, strychnos nux-vomica seed, phytolacca americana root, pulsatilla vulgaris) pellets is temporary relieves cold symptoms such as sneezing, runny nose, nasal congestion and minor sore throat. This formulation utilizes a pellet delivery system. Marketed by Laboratoires Boiron, this product is identified by NDC 0220-9049.
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Allergens - [CS]
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Vegetable Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 0220 - Laboratoires Boiron
- 0220-9049 - Children Coldcalm
- 0220-9049-42 - 1 TUBE in 1 BOX / 80 PELLET in 1 TUBE (0220-9049-41)
- 0220-9049 - Children Coldcalm
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 0220-9049-42 identifies a specific commercial package of 1 tube in 1 box / 80 pellet in 1 tube (0220-9049-41) of Children Coldcalm, a human over the counter drug labeled by Laboratoires Boiron. This pellet is formulated for oral use and contains apis mellifera; atropa belladonna; eupatorium perfoliatum flowering top; gelsemium sempervirens root; onion; phytolacca americana root; potassium dichromate; pulsatilla vulgaris; strychnos nux-vomica seed 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 Laboratoires Boiron on September 08, 2008. The current certification is valid through December 31, 2026.
How is this Laboratoires Boiron product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00220904942. 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 Labeler segment to maintain the 5-4-2 structure.