P-10, r. 15 - Regulation respecting the labelling of medications and poisons

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chapter P-10, r. 15
Regulation respecting the labelling of medications and poisons
Pharmacy Act
(chapter P-10, s. 10, 1st par., subpar. c).
DIVISION I
GENERAL PROVISION
1.01. The Interpretation Act (chapter I-16) applies to this Regulation.
R.R.Q., 1981, c. P-10, r. 11, s. 1.01.
DIVISION II
MEDICATIONS
2.01. Every pharmacist must, in the practice of his profession, enter the following information on the label identifying a medication prepared or sold under a prescription:
(a)  patient: name;
(b)  medication prescribed:
i.  date of dispensing and number of the prescription;
ii.  generic or trade name;
iii.  quantity and concentration of the medication;
iv.  dosage;
v.  directions for use of the medication, if any;
vi.  special directions for preservation of the medication, if any;
vii.  authorized renewal;
viii.  special precautions, if any; and
ix.  expiration date of the medication, if any;
(c)  prescribing physician: name;
(d)  identification of pharmacist: name, address and telephone number of the pharmacist who is the owner.
However, in the case of a pharmacist practising in an institution within the meaning of the Act respecting health services and social services (chapter S-4.2) or the Act respecting health services and social services for Cree Native persons (chapter S-5), the inscription of the prescription number is optional and the identification of the pharmacist may be replaced by the identification of the institution.
R.R.Q., 1981, c. P-10, r. 11, s. 2.01; Decision 81-12-15, s. 1.
2.02. Every pharmacist must, in the practice of his profession, enter the following information on the label identifying a medication prepared or sold without a prescription:
(a)  medication:
i.  generic or trade name, concentration and quantity of the medication;
ii.  average dosage for adult or child;
iii.  directions for use of the medication, if any;
iv.  special directions for preservation of the medication, if any;
v.  expiration date of the medication, if any; and
vi.  special precautions, if any;
(b)  identification of pharmacist: name, address and telephone number of the pharmacist who is the owner.
R.R.Q., 1981, c. P-10, r. 11, s. 2.02.
2.03. Section 2.02 shall not apply to medications delivered to the patient in the original container of the manufacturer.
R.R.Q., 1981, c. P-10, r. 11, s. 2.03.
DIVISION III
POISONS
3.01. Every pharmacist must, in the practice of his profession, enter the following information on the label identifying a poison:
(a)  poison:
i.  special precautions, in particular the inscription of the word “poison”;
ii.  name of the poison, quantity and concentration;
iii.  instructions in case of intoxication;
iv.  special directions for preservation, if any; and
v.  directions for use, if any, according to the intentions expressed by the patient;
(b)  identification of the pharmacist: name, address and telephone number of the pharmacist who is the owner.
R.R.Q., 1981, c. P-10, r. 11, s. 3.01.
3.02. Section 3.01 shall not apply to poisons delivered in the original container of the manufacturer.
R.R.Q., 1981, c. P-10, r. 11, s. 3.02.
REFERENCES
R.R.Q., 1981, c. P-10, r. 11
Decision 81-12-15, 1982 G.O. 2, 2052; Suppl. 1016