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- Product NDC
- 69968-0053
- 11-digit product format
- 699680053
- Labeler code
- 69968
- Product ID
- 69968-0053_cdd4de8b-093e-ae93-e053-2a95a90a4528
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE and PRAMOXINE HYDROCHLORIDE
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Johnson & Johnson Consumer Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-06-01
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE; PRAMOXINE HYDROCHLORIDE
- Active strength
- 1 mg/mL; mg/mL
- 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 |
|---|
| 69968-0053-1 | 69968005301 | 1 VIAL in 1 BLISTER PACK (69968-0053-1) > 7.7 mL in 1 VIAL | 1 vial | 2018-06-01 | 0000-00-00 | No | No | Current |