Orbitol Whitening
- Product NDC
- 69939-129
- 11-digit product format
- 699390129
- Labeler code
- 69939
- Product ID
- 69939-129_9321ffab-85c1-4d45-a713-8c5e7ac85f6d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- COSMOPHARM LTD
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-04-13
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 g/100g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record