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# Raritan Pharmaceuticals Recalls Products Containing Belladonna Extract
- URL: https://www.foodconsumer.org/belladonna_extract_1125160230/
- Published: 2016-11-25T15:23:00.000Z
- Updated: 2026-09-22T16:31:16.000Z
- Description: Raritan Pharmaceuticals is recalling homeopathic products it makes for Homeolab USA, including CVS infants' teething tablets and two children's ear relief liquids, because FDA testing found belladonna extract at levels that varied from the label. Consumers should stop using the listed lots.
- Author: Food Consumer
- Tags: Drug, Health News, #vivvo-import

### MedWatch - The FDA Safety Information and Adverse Event Reporting Program

Products Containing Belladonna Extract by Raritan Pharmaceuticals: Recall - Possible Belladonna Alkaloids

**AUDIENCE**: Consumer, Pharmacy, Pain management, Family Practice, Pediatrics

**ISSUE**: Raritan Pharmaceuticals, a contract manufacturer for Homeolab USA, is voluntarily recalling homeopathic products containing [belladonna](https://medlineplus.gov/druginfo/natural/531.html?ref=foodconsumer.org) extract (see products below) due to the potential for variation in the content of belladonna extract in the products. The FDA has tested some products and recovered varying levels of belladonna extract content from what is declared on the label.

**BACKGROUND**: Raritan Pharmaceuticals is a contract manufacturer of these products for Homeolab USA that supplies the belladonna blends to Raritan Pharmaceuticals. These products were distributed Nationwide: 1) Product: CVS Homeopathic Infants' Teething Tablet 135 tablets, UPC: 050428424162, Lots: 41116 and 43436; 2) Product: Kids Relief Homeopathic Ear Relief Oral Liquid 0.85 fl. oz., UPC: 778159090639, Lot: 35254 3) Product: CVS Homeopathic Kids' Ear Relief Liquid 0.85 fl. oz., UPC: 050428441633, Lot: 33149.

**RECOMMENDATION**: Consumers with any product being recalled should stop using the product. Consumers with questions regarding this recall can contact Raritan Pharmaceuticals by phone at [1-866-467-2748](tel:1-866-467-2748) (Monday-Friday from 8am to 5:30pm EST). Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:

- Complete and submit the report Online: [www.fda.gov/MedWatch/report](http://links.govdelivery.com/track?type=click&enid=ZWFzPTEmbWFpbGluZ2lkPTIwMTYxMTI1LjY2ODE4NTcxJm1lc3NhZ2VpZD1NREItUFJELUJVTC0yMDE2MTEyNS42NjgxODU3MSZkYXRhYmFzZWlkPTEwMDEmc2VyaWFsPTE3MzY2NzY0JmVtYWlsaWQ9Zm9vZGNvbnN1bWVyLm9yZ0BnbWFpbC5jb20mdXNlcmlkPWZvb2Rjb25zdW1lci5vcmdAZ21haWwuY29tJmZsPSZleHRyYT1NdWx0aXZhcmlhdGVJZD0mJiY=&&&100&&&http://www.fda.gov/MedWatch/report?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery)
- [Download form ](http://links.govdelivery.com/track?type=click&enid=ZWFzPTEmbWFpbGluZ2lkPTIwMTYxMTI1LjY2ODE4NTcxJm1lc3NhZ2VpZD1NREItUFJELUJVTC0yMDE2MTEyNS42NjgxODU3MSZkYXRhYmFzZWlkPTEwMDEmc2VyaWFsPTE3MzY2NzY0JmVtYWlsaWQ9Zm9vZGNvbnN1bWVyLm9yZ0BnbWFpbC5jb20mdXNlcmlkPWZvb2Rjb25zdW1lci5vcmdAZ21haWwuY29tJmZsPSZleHRyYT1NdWx0aXZhcmlhdGVJZD0mJiY=&&&101&&&http://www.fda.gov/Safety/MedWatch/HowToReport/DownloadForms/default.htm?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery)or call [1-800-332-1088](tel:1-800-332-1088) to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

Read the MedWatch safety alert, including links to the Recall notice at:

[http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm530642.htm](http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm530642.htm?ref=foodconsumer.org)