Katinko Pain And Itch Relieving
- Product NDC
- 52241-300
- 11-digit product format
- 522410300
- Labeler code
- 52241
- Product ID
- 52241-300_5741c85f-da5d-402e-888d-6daea61ad6cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
- Dosage form
- STICK
- Route
- TOPICAL
- Labeler
- Greenstone Pharmaceutical H.K. Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-05-24
- Marketing end
- 0000-00-00
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
- Active strength
- 11 g/100g; g/100g; g/100g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2019-12-08 06:16 UTC · source 2019-12-05 | excluded product | product | 52241-300 | E | Excluded after deficient or non-compliant submission was not corrected | excluded / ndc_excluded.zip | 110d247fa046… | a55b01930146… | ||
| 2019-12-08 06:16 UTC · source 2019-12-05 | excluded package | package | 52241-300 | 52241-300-12 | E | Excluded after deficient or non-compliant submission was not corrected | excluded / ndc_excluded.zip | 110d247fa046… | a55b01930146… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.