BIO SPECTRA
- Product NDC
- 61649-398
- 11-digit product format
- 616490398
- Labeler code
- 61649
- Product ID
- 61649-398_076c39b9-0900-42dc-8249-f30a8a155491
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- BIO SPECTRA
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-11-15
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 72 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 61649-398-01 | 61649039801 | 100 mL in 1 BOTTLE, SPRAY (61649-398-01) | 100 ml | 2020-11-15 | 0000-00-00 | No | No | Current |
| 61649-398-02 | 61649039802 | 473 mL in 1 BOTTLE, PLASTIC (61649-398-02) | 473 ml | 2020-11-15 | 0000-00-00 | No | No | Current |