Motion Sickness Relief
- Product NDC
- 63868-034
- 11-digit product format
- 638680034
- Labeler code
- 63868
- Product ID
- 63868-034_eacbb50a-3b71-4eda-b08f-ee400f88c956
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dimenhydrinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CHAIN DRUG MARKETING ASSOCIATION INC
- Application
- part336
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 1992-12-01
- Marketing end
- 0000-00-00
- Substance
- DIMENHYDRINATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 63868-034 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 63868-034 | 63868-034-12 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 63868-034 | 63868-034-24 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63868-034-12 | EA - Each | 63868-034 | 3107aef5-88b4-431c-816a-6e01abf84bee | 1 | 2022-10-06 |
| 63868-034-24 | EA - Each | 63868-034 | 6847bcaf-5bf4-4c6a-9e24-611c39932685 | 1 | 2022-10-06 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| DIMENHYDRINATE | ACTIVE INGREDIENT | JB937PER5C | MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [CHAIN DRUG MARKETING ASSOCIATION INC] | 1 | |
| DIPHENHYDRAMINE | ACTIVE MOIETY | 8GTS82S83M | MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [CHAIN DRUG MARKETING ASSOCIATION INC] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [CHAIN DRUG MARKETING ASSOCIATION INC] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [CHAIN DRUG MARKETING ASSOCIATION INC] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [CHAIN DRUG MARKETING ASSOCIATION INC] | 1 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [CHAIN DRUG MARKETING ASSOCIATION INC] | 1 |
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63868-034-12 | 63868003412 | 2 BLISTER PACK in 1 CARTON (63868-034-12) > 6 TABLET in 1 BLISTER PACK | 2 blister pack | 1992-12-01 | 0000-00-00 | No | No | Current |
| 63868-034-24 | 63868003424 | 4 BLISTER PACK in 1 CARTON (63868-034-24) > 6 TABLET in 1 BLISTER PACK | 4 blister pack | 1992-12-01 | 0000-00-00 | No | No | Current |