Agency Information Collection Activities: Proposed Collection; Comment Request; Bar Code Label Requirement for Human Drug and Biological Products; Correction

---
identifier: "/us/fr/2015-32252"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Agency Information Collection Activities: Proposed Collection; Comment Request; Bar Code Label Requirement for Human Drug and Biological Products; Correction"
title_number: 0
title_name: "Federal Register"
section_number: "2015-32252"
section_name: "Agency Information Collection Activities: Proposed Collection; Comment Request; Bar Code Label Requirement for Human Drug and Biological Products; Correction"
positive_law: false
currency: "2015-12-23"
last_updated: "2015-12-23"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "2015-32252"
document_type: "notice"
publication_date: "2015-12-23"
agencies:
  - "Health and Human Services Department"
  - "Food and Drug Administration"
fr_citation: "80 FR 79912"
fr_volume: 80
docket_ids:
  - "Docket No. FDA-2012-N-0873"
fr_action: "Notice; correction."
---


#  Agency Information Collection Activities: Proposed Collection; Comment Request; Bar Code Label Requirement for Human Drug and Biological Products; Correction

**AGENCY:**

Food and Drug Administration, HHS.

**ACTION:**

Notice; correction.

**SUMMARY:**

The Food and Drug Administration (FDA) is correcting a notice entitled “Agency Information Collection Activities: Proposed Collection; Comment Request; Bar Code Label Requirement for Human Drug and Biological Products” that appeared in the *Federal Register* of December 15, 2015 (80 FR 77637). The document solicited comments on the bar code label requirements for human drug and biological products. The document was published with an incorrect docket number. This document corrects that error.

**FOR FURTHER INFORMATION CONTACT:**

Lisa Granger, Office of Policy and Planning, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 32, rm. 3330, Silver Spring, MD 20993-0002, 301-796-9115.

**SUPPLEMENTARY INFORMATION:**

In the *Federal Register* of Tuesday, December 15, 2015, in FR Doc. 2015-31402, the following correction is made:

1. On page 77637, in the second column, the docket number is corrected to read FDA-2012-N-0873.

Dated: December 15, 2015.

Leslie Kux,

Associate Commissioner for Policy.