FDA Label for Betaine Anhydrous
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Betaine Anhydrous Product Label
The following document was submitted to the FDA by the labeler of this product Eton Pharmaceuticals, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
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No current SPL for Eton. See Betaine Anhydrous for Oral Solution - betaine powder, for solution NDC Code: 55792-002-01
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ef44452a-5707-0d39-cbba-2fa285fb994c
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