§ 111.160 What requirements apply to packaging and labels received?
(a)Youmust visually examine each immediate container or grouping of immediate containers in a shipment for appropriate content label, container damage, or broken seals to determine whether the container condition may have resulted in contamination or deterioration of the packaging and labels.
(b)Youmust visually examine the supplier's invoice, guarantee, or certification in a shipment to ensure that the packaging or labels are consistent with your purchase order.
(c)Youmust quarantine packaging and labels before you use them in the manufacture of a dietary supplement until:
(1)You collect representative samples of each unique shipment, and of each unique lot within each unique shipment, of packaging and labels and, at a minimum, conduct a visual identification of the immediate containers and closures;
(2)Quality control personnel review and approve the results of any tests or examinations conducted on the packaging and labels; and
(3)Quality control personnel approve the packaging and labels for use in the manufacture of a dietary supplement and release them from quarantine.
(1)Youmust identify each unique lot within each unique shipment of packaging and labels in a manner that allows you to trace the lot to the supplier, the date received, the name of the packaging and label, the status of the packaging and label (e.g., quarantined, approved, or rejected); and to the dietary supplement that you distributed; and
(2)Youmust use this unique identifier whenever you record the disposition of each unique lot within each unique shipment of packaging and labels.
(e)Youmust hold packaging and labels under conditions that will protect against contamination and deterioration, and avoid mixups.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.