Neora
- Product NDC
- 72935-001
- Requested package NDC
- 72935-001-45
- 11-digit product format
- 729350001
- Labeler code
- 72935
- Product ID
- 72935-001_82e875ec-aa03-8b57-e053-2991aa0a859d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic acid
- Dosage form
- SWAB
- Route
- TOPICAL
- Labeler
- Neora, LLC
- Application
- part333D
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-05-01
- Marketing end
- 0000-00-00
- Substance
- SALICYLIC ACID
- Active strength
- 1 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 72935-001-45 | 72935000145 | 1 JAR in 1 CARTON (72935-001-45) > 45 APPLICATOR in 1 JAR > 1.1 mL in 1 APPLICATOR | 1 jar | 2019-05-01 | 0000-00-00 | No | No | Current |