Regulatory Updates
Revision of the standards and specifications for foods and food additives under the Food Sanitation Law (Additional establishment of residue limits for veterinary drug)
Distribution date: 29 June 2007 | Final date for Comment: 28 August 2007
Withdrawal of the maximum residue limits for avoparcin (Feed additive and veterinary drug) on all commodities listed under Item 3.
Products Covered: Cattle (muscle, fat, liver, kidney and other edible offal), pig (muscle, fat, liver, kidney and other edible offal), other terrestrial mammals (muscle, fat, liver, kidney and other edible offal), milk, chicken (muscle, fat, liver, kidney and other edible offal), other poultry (muscle, fat, liver, kidney and other edible offal)
Regulation Type: Regular notification
Revision of the standards and specifications for foods and food additives under the Food Sanitation Law (Additional establishment of residue limits for veterinary drug)
Distribution date: 29 June 2007 | Final date for Comment: 28 August 2007
Withdrawal of the maximum residue limits for avoparcin (Feed additive and veterinary drug) on all commodities listed under Item 3.
Products Covered: Cattle (muscle, fat, liver, kidney and other edible offal), pig (muscle, fat, liver, kidney and other edible offal), other terrestrial mammals (muscle, fat, liver, kidney and other edible offal), milk, chicken (muscle, fat, liver, kidney and other edible offal), other poultry (muscle, fat, liver, kidney and other edible offal)
Regulation Type: Regular notification
Revision of the standards and specifications for foods and food additives under the Food Sanitation Law (Additional establishment of residue limits for veterinary drug)
Distribution date: 29 June 2007 | Final date for Comment: 28 August 2007
Establishment of maximum residue limits for veterinary drug, difloxacin, in foods
Products Covered: Pig (muscle, fat, liver, kidney and other edible offal)
Regulation Type: Regular notification
Revision of the standards and specifications for foods and food additives under the Food Sanitation Law (Additional establishment of residue limits for veterinary drug)
Distribution date: 29 June 2007 | Final date for Comment: 28 August 2007
Establishment of maximum residue limits for veterinary drug, difloxacin, in foods
Products Covered: Pig (muscle, fat, liver, kidney and other edible offal)
Regulation Type: Regular notification
Revision of the standards and specifications for foods and food additives under the Food Sanitation Law (Additional establishment of residue limits for veterinary drug)
Distribution date: 29 June 2007 | Final date for Comment: 28 August 2007
Establishment of maximum residue limits for veterinary drug, dramectin, in foods.
Products Covered: Cattle (muscle, fat, liver, kidney and other edible offal), pig (muscle, fat, liver, kidney and other edible offal), other terrestrial mammals (muscle, fat, liver, kidney and other edible offal), milk
Regulation Type: Regular notification
Revision of the standards and specifications for foods and food additives under the Food Sanitation Law (Additional establishment of residue limits for veterinary drug)
Distribution date: 29 June 2007 | Final date for Comment: 28 August 2007
Establishment of maximum residue limits for veterinary drug, dramectin, in foods.
Products Covered: Cattle (muscle, fat, liver, kidney and other edible offal), pig (muscle, fat, liver, kidney and other edible offal), other terrestrial mammals (muscle, fat, liver, kidney and other edible offal), milk
Regulation Type: Regular notification
Partial revision of the Japanese Pharmacopoeia Fifteenth edition (6 pages, in English).
Distribution date: 27 June 2007
Products Covered: Drugs (HS: 30)
Regulation Type: Regular notification
Partial revision of the Japanese Pharmacopoeia Fifteenth edition (6 pages, in English).
Distribution date: 27 June 2007
Products Covered: Drugs (HS: 30)
Regulation Type: Regular notification
Listing of Color Additives Subject to Certification; D&C Black No. 3 (4 pages, in English).
Distribution date: 26 June 2007
The Food and Drug Administration (FDA) is amending the colour additive regulations to provide for the safe use of D&C Black No. 3 (bone black, subject to FDA batch certification) as a colour additive in eyeliner, eye shadow, mascara, and face powder. This rule is effective 20 July 2007. Submit written or electronic objections and requests for a hearing by 19 July 2007.
Products Covered: Eyeliner, eye shadow, mascara, and face powder (HS: 3304; ICS: 71.100)
Regulation Type: Regular notification
Listing of Color Additives Subject to Certification; D&C Black No. 3 (4 pages, in English).
Distribution date: 26 June 2007
The Food and Drug Administration (FDA) is amending the colour additive regulations to provide for the safe use of D&C Black No. 3 (bone black, subject to FDA batch certification) as a colour additive in eyeliner, eye shadow, mascara, and face powder. This rule is effective 20 July 2007. Submit written or electronic objections and requests for a hearing by 19 July 2007.
Products Covered: Eyeliner, eye shadow, mascara, and face powder (HS: 3304; ICS: 71.100)
Regulation Type: Regular notification
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