Indian Herb Paste
Unapproved new drug
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Unapproved new drug
Cause type: Unapproved drug
The product was marketed without an approved NDA/ANDA, or does not meet the OTC monograph it claims to follow. Nothing about the product - dose, purity, safety - has been reviewed by FDA, so the claims on the box are unverified. All unapproved drug recalls.
Life-Line tm Catalytic Activated Energy Water, 1 gallon container, McDaniel Life-Line LLC 1775 US Hwy 385 806-647-1741 Dimmitt, TX 79027
Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.
Unapproved new drug
Marketed without an Approved NDA/ANDA; FDA analysis found product to contain tadalfil
Marketed without an Approved NDA/ANDA; FDA analysis found product to contain tadalfil
Marketed without an Approved NDA/ANDA; FDA analysis found product to contain tadalfil
Marketed without an Approved NDA/ANDA; FDA analysis found product to contain tadalfil
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