• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Drugs

  • Print
  • Share
  • E-mail

Rulemaking History for OTC Poison Treatment Drug Products

Pending Final Monograph (21 CFR part 337):  
Emetic Drug Products for Over-the-Counter Human Use

Pending Final Monograph (21 CFR part 357 subpart A):  
Miscellaneous Internal Drug Products for Over-the-Counter Human Use: Treatment of Acute Toxic Ingestion

OTC Poison Treatment Drug Products found on this page:


Poison Treatment Drug Products: Emetic
Advance Notice Of Proposed Rulemaking Date FR Citation
Advance Notice of Proposed Rulemaking: Ipecac syrup [PDF] 3/21/1975 40FR12902
Proposed Rule Date FR Citation
Tentative Final Monograph [PDF] 9/5/1978 43FR39544
    Correction [PDF] 11/28/1978 43FR55417
 
Poison Treatment Drug Products: Nonmonograph Ingredients
Proposed Rule Date FR Citation
Proposed Rule: Classifies category II and III ingredients without data as nonmonograph [PDF] 5/16/1990 55FR20434
    Correction 6/7/1990 55FR23235
Final Rule Date FR Citation
Final Rule: Classifies category II and III ingredients without data as nonmonograph [PDF] 11/7/1990 55FR46914
    Correction [PDF] 12/3/1990 55FR49973
    Technical Amendment: Corrects an ingredient name [PDF] 1/30/1992 57FR3526
 
Poison Treatment Drug Products: Acute Toxic Ingestion
Advance Notice Of Proposed Rulemaking Date FR Citation
Advance Notice of Proposed Rulemaking: Ipecac syrup and activated charcoal [PDF] 1/5/1982 47FR444
Proposed Rule Date FR Citation
Tentative Final Monograph [PDF] 1/15/1985 50FR2244
    Correction [PDF] 2/15/1985 50FR6359
    Correction [PDF] 3/6/1985 50FR9040
Notice: Advisory Committee Meeting, Ipecac Syrup [PDF] 5/6/2003 68FR24004