Motion Sickness Relief
- Product NDC
- 21130-198
- 11-digit product format
- 211300198
- Labeler code
- 21130
- Product ID
- 21130-198_861617dd-7274-43c7-a69c-472280a463bc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dimenhydrinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Better Living Brands, LLC
- Application
- part336
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 1992-12-01
- Marketing end
- 2019-07-18
- Substance
- DIMENHYDRINATE
- Active strength
- 50 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record