Colic Drops Liquid
NDC Package 63083-2155-2
Package Information
Colic Drops liquids is for temporary relief of irritability or abdominal tenderness, minor pain, or cramping.*. This formulation utilizes a liquid delivery system. Marketed by Professional Complementary Health Formulas, this product is identified by NDC 63083-2155.
Identification & Billing
Clinical Specifications
- ALUMINUM OXIDE 12 [hp_X]/59mL
- BRYONIA ALBA ROOT 4 [hp_X]/59mL
- CASANTHRANOL 30 [hp_X]/59mL
- CITRULLUS COLOCYNTHIS FRUIT PULP 6 [hp_X]/59mL
- LACHESIS MUTA VENOM 30 [hp_X]/59mL
- LEAD 12 [hp_X]/59mL
- LYCOPODIUM CLAVATUM SPORE 4 [hp_X]/59mL
- MERCURIC CHLORIDE 12 [hp_X]/59mL
- SENNA LEAF 30 [hp_X]/59mL
- STRYCHNOS NUX-VOMICA SEED 4 [hp_X]/59mL
- SULFUR 12 [hp_X]/59mL
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 63083 - Professional Complementary Health Formulas
- 63083-2155 - Colic Drops
- 63083-2155-2 - 59 mL in 1 BOTTLE, DROPPER
- 63083-2155 - Colic Drops
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.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 63083-2155-2 identifies a specific commercial package of 59 ml in 1 bottle, dropper of Colic Drops 2155, a human over the counter drug labeled by Professional Complementary Health Formulas. This liquid is formulated for oral use and contains aluminum oxide; bryonia alba root; casanthranol; citrullus colocynthis fruit pulp; lachesis muta venom; lead; lycopodium clavatum spore; mercuric chloride; senna leaf; strychnos nux-vomica seed; sulfur 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 Professional Complementary Health Formulas on August 15, 1984. The current certification is valid through December 31, 2027.
How is this Professional Complementary Health Formulas product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 63083215502. 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.