Nighty Nite
- Product NDC
- 49304-0020
- 11-digit product format
- 493040020
- Labeler code
- 49304
- Product ID
- 49304-0020_09c56e7a-7a80-4369-a4bb-6a57ef7d5f94
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- NOT APPLICABLE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Alternative Pharmacy
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-09-05
- Marketing end
- 0000-00-00
- Substance
- GRINDELIA HIRSUTULA WHOLE; MELATONIN; PASSIFLORA INCARNATA FLOWERING TOP
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#