Stellalife Vega Oral Care Spray
NDC Package 61727-101-01
Package Information
Stellalife Vega Oral Care (spray) sprays is a human otc drug administered via dental; sublingual route. This formulation utilizes a spray delivery system. Marketed by Homeocare Laboratories, Inc., this product is identified by NDC 61727-101.
Identification & Billing
Clinical Specifications
- Dental - Administration to a tooth or teeth.
- Sublingual - Administration beneath the tongue.
- ACONITUM NAPELLUS 3 [hp_X]/mL
- ARNICA MONTANA 18 [hp_X]/mL
- CALCIUM SULFIDE 8 [hp_X]/mL
- CALENDULA OFFICINALIS FLOWERING TOP 3 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
- ECHINACEA PURPUREA 3 [hp_X]/mL
- GELSEMIUM SEMPERVIRENS ROOT 30 [hp_X]/mL
- HYPERICUM PERFORATUM 10 [hp_X]/mL
- MATRICARIA RECUTITA 5 [hp_X]/mL
- MERCURY 10 [hp_X]/mL
- RUTA GRAVEOLENS FLOWERING TOP 12 [hp_X]/mL
- STRYCHNOS IGNATII SEED 30 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 61727 - Homeocare Laboratories, Inc.
- 61727-101 - Stellalife Vega Oral Care
- 61727-101-01 - 1 BOTTLE, SPRAY in 1 BOX / 30 mL in 1 BOTTLE, SPRAY
- 61727-101 - Stellalife Vega Oral Care
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 61727-101-01 identifies a specific commercial package of 1 bottle, spray in 1 box / 30 ml in 1 bottle, spray of Stellalife Vega Oral Care, a human over the counter drug labeled by Homeocare Laboratories, Inc.. This spray is formulated for dental; sublingual use and contains aconitum napellus; arnica montana; calcium sulfide; calendula officinalis flowering top; echinacea angustifolia; echinacea purpurea; gelsemium sempervirens root; hypericum perforatum; matricaria recutita; mercury; ruta graveolens flowering top; strychnos ignatii 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 Homeocare Laboratories, Inc. on December 10, 2016. The current certification is valid through December 31, 2026.
How is this Homeocare Laboratories, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 61727010101. 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.