7th MANNA PAIN RELIEF DROPS
- Product NDC
- 71856-423
- 11-digit product format
- 718560423
- Labeler code
- 71856
- Product ID
- 71856-423_09dc19d0-24b9-bd12-e063-6294a90ab40f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, CAMPHOR (SYNTHETIC)
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- 7TH MANNA (USA) PTE. LTD.
- Application
- M017B
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-09-25
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL
- Active strength
- 30; 100 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- 7th MANNA PAIN RELIEF DROPS
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CAMPHOR (SYNTHETIC) | 30 mg/mL |
| MENTHOL | 100 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5TJD82A1ET, L7T10EIP3A |
| Rxcui | 1987413 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71856-423-00 | 7th MANNA PAIN RELIEF DROPS | 1 in 1 BOX | LIQUID | 1 | | 2 |
| 71856-423-00 | 7th MANNA PAIN RELIEF DROPS | 30 mL in 1 BOTTLE | LIQUID | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71856-423 | 7TH MANNA PAIN RELIEF DROPS (MENTHOL, CAMPHOR (SYNTHETIC)) LIQUID [7TH MANNA (USA) PTE. LTD.] | 2 | Current NDC, 2 package rows | 20231112_699c668c-4f54-4f18-b585-bdcebe7a2c4e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71856-423-00 | 71856042300 | 1 BOTTLE in 1 BOX (71856-423-00) / 30 mL in 1 BOTTLE | 1 bottle | 2023-09-25 | No | No | Current |