BIO SPECTRA
- Product NDC
- 61649-317
- 11-digit product format
- 616490317
- Labeler code
- 61649
- Product ID
- 61649-317_f618d4b2-7c88-4df3-b435-d3920862c132
- 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 |
|---|
| 61649-317-01 | 61649031701 | 100 mL in 1 BOTTLE, SPRAY (61649-317-01) | 100 ml | 2020-11-15 | 0000-00-00 | No | No | Current |
| 61649-317-02 | 61649031702 | 473 mL in 1 BOTTLE, PLASTIC (61649-317-02) | 473 ml | 2020-11-15 | 0000-00-00 | No | No | Current |