Neosporin Original
- Product NDC
- 58232-4002
- 11-digit product format
- 582324002
- Labeler code
- 58232
- Product ID
- 58232-4002_cb1603c2-e8eb-b459-e053-2995a90aec60
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Johnson & Johnson Consumer Inc.
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-08-03
- Marketing end
- 0000-00-00
- Substance
- BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
- Active strength
- 400 [iU]/g; mg/g; [iU]/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58232-4002-1 | 58232400201 | .9 g in 1 POUCH (58232-4002-1) | | 2011-08-03 | 0000-00-00 | No | No | Current |
| 58232-4002-8 | 58232400208 | .9 g in 1 POUCH (58232-4002-8) | | 2011-08-03 | 0000-00-00 | No | No | Current |
| 58232-4002-9 | 58232400209 | 144 POUCH in 1 CARTON (58232-4002-9) > .9 g in 1 POUCH | 144 pouch | 2011-08-03 | 0000-00-00 | No | No | Current |