Data / Drug companies / Homeolab International (Canada) Inc
Homeolab International (Canada) Inc: 23 products in the FDA NDC directory, labeler code 71971
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Homeolab International (Canada) Inc (labeler code 71971) lists 23 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 23 over the counter drugs. Its main marketing category is unapproved homeopathic products. The newest product started marketing on September 1, 2022.
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- Labeler code
- 71971
- Products in commercial distribution
- 23
- Packages
- 46
- Finished drugs by generic name
- 1
- Prescription products
- 0
- Over the counter products
- 23
- Flagged as original packager
- 17 of 17 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- March 3, 2017
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Unapproved homeopathic products | 23 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 23 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Anas barbariae hepatis et cordis | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Liquid | 16 | 69.6% |
| Tablet | 5 | 21.7% |
| Kit | 2 | 8.7% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Real Relief Natural Wellness Calming Syrup | 71971-9042 | Liquid | Unapproved homeopathic products | September 1, 2022 |
| Real Relief Natural Wellness Cough and Cold Syrup Combo Pack Daytime Formula and Nighttime Formula | 71971-6155 | Kit | Unapproved homeopathic products | September 1, 2022 |
| Kids Relief Cough and Cold Syrup Combo Pack Daytime Formula and Nighttime Formula | 71971-6105 | Kit | Unapproved homeopathic products | September 1, 2022 |
| Real Relief | 71971-6036 | Tablet | Unapproved homeopathic products | January 1, 2020 |
| Real Relief | 71971-6032 | Tablet | Unapproved homeopathic products | January 1, 2020 |
| Real Relief | 71971-6030 | Tablet | Unapproved homeopathic products | January 1, 2020 |
| Real Relief | 71971-6002 | Tablet | Unapproved homeopathic products | January 1, 2020 |
| Real Relief | 71971-6001 | Tablet | Unapproved homeopathic products | January 1, 2020 |
| Kids Relief | 71971-9021 | Liquid | Unapproved homeopathic products | August 1, 2019 |
| Kids Relief | 71971-9066 | Liquid | Unapproved homeopathic products | July 26, 2019 |
| Kids Relief | 71971-9999 | Liquid | Unapproved homeopathic products | May 3, 2018 |
| Real Relief | 71971-9899 | Liquid | Unapproved homeopathic products | May 3, 2018 |
| Real Relief | 71971-9204 | Liquid | Unapproved homeopathic products | March 3, 2018 |
| Real Relief | 71971-9185 | Liquid | Unapproved homeopathic products | March 3, 2018 |
| Kids Relief | 71971-9151 | Liquid | Unapproved homeopathic products | March 3, 2018 |
| Kids Relief | 71971-9121 | Liquid | Unapproved homeopathic products | March 3, 2018 |
| Kids Relief | 71971-9104 | Liquid | Unapproved homeopathic products | March 3, 2018 |
| Kids Relief | 71971-9216 | Liquid | Unapproved homeopathic products | March 3, 2017 |
| Kids Relief | 71971-9214 | Liquid | Unapproved homeopathic products | March 3, 2017 |
| Kids Relief | 71971-9083 | Liquid | Unapproved homeopathic products | March 3, 2017 |
| Kids Relief | 71971-9077 | Liquid | Unapproved homeopathic products | March 3, 2017 |
| Kids Relief | 71971-9062 | Liquid | Unapproved homeopathic products | March 3, 2017 |
| Kids Relief Teething Oral Liquid | 71971-9060 | Liquid | Unapproved homeopathic products | March 3, 2017 |
CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.