antibiotic plus pain relief
- Product NDC
- 11822-0637
- Requested package NDC
- 11822-0637-1
- 11-digit product format
- 118220637
- Labeler code
- 11822
- Product ID
- 11822-0637_356bfcb1-8c4c-4464-889f-f2e4dd322109
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Neomycin, Polymyxin B, Pramoxine HCl
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Rite Aid Corporation
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2005-07-14
- Marketing end
- 0000-00-00
- Substance
- NEOMYCIN SULFATE; PRAMOXINE HYDROCHLORIDE; POLYMYXIN B SULFATE
- Active strength
- 4 mg/g; mg/g; [USP'U]/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 11822-0637 | 11822-0637-1 | D | Discontinued by firm | 2026-10-16 |
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.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 11822-0637 | 11822-0637-1 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 11822-0637 | 11822-0637-1 | D | Discontinued by firm | excluded / ndc_excluded.zip | f5e01cc5f278… | a2eaf40c39c3… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 11822-0637-1 | 11822063701 | 1 TUBE in 1 CARTON (11822-0637-1) > 14 g in 1 TUBE | 1 tube | 2005-07-14 | 0000-00-00 | No | No | Current |