ULTRA SEAL Triple Antibiotic
- Product NDC
- 42213-360
- 11-digit product format
- 422130360
- Labeler code
- 42213
- Product ID
- 42213-360_9626a7c9-b05f-b11d-e053-2a95a90a7707
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- neomycin, polymixin, bacitracin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Ultra Seal Corporation
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-04-12
- Marketing end
- 0000-00-00
- Substance
- NEOMYCIN SULFATE; POLYMYXIN B SULFATE; BACITRACIN ZINC
- Active strength
- 5 mg/g; [iU]/g; [iU]/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 42213-360-28 | 42213036028 | 1 TUBE in 1 CARTON (42213-360-28) > 28 g in 1 TUBE | 1 tube | 2019-09-05 | 0000-00-00 | No | No | Current |
| 42213-360-80 | 42213036080 | 144 PACKET in 1 BOX (42213-360-80) > .9 g in 1 PACKET (42213-360-09) | 144 packet | 2019-09-05 | 0000-00-00 | No | No | Current |