Triple Antibiotic Plus Pain Relief

Product NDC
67510-1670
11-digit product format
675101670
Labeler code
67510
Product ID
67510-1670_9ee421b7-bbd7-6d33-e053-2a95a90a2b47
Type
HUMAN OTC DRUG
Nonproprietary name
Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Kareway Product, Inc.
Application
part333B
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-07-26
Marketing end
0000-00-00
Substance
NEOMYCIN SULFATE; PRAMOXINE HYDROCHLORIDE; BACITRACIN ZINC; POLYMYXIN B SULFATE
Active strength
4 mg/g; mg/g; [iU]/g; [iU]/g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Dataset, Scope, Package NDC table
DatasetScopePackage NDC
excluded productproduct
excluded packagepackage67510-1670-1
excluded packagepackage67510-1670-5
excluded packagepackage67510-1670-3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
67510-1670-1675101670011 TUBE in 1 CARTON (67510-1670-1) > 28.3 g in 1 TUBE1 tube2017-07-260000-00-00NoNoCurrent
67510-1670-3675101670031 TUBE in 1 CARTON (67510-1670-3) > 9.4 g in 1 TUBE1 tube2017-07-260000-00-00NoNoCurrent
67510-1670-5675101670051 TUBE in 1 CARTON (67510-1670-5) > 14 g in 1 TUBE1 tube2017-07-260000-00-00NoNoCurrent