Peppermint Aqua
- Product NDC
- 76845-101
- 11-digit product format
- 768450101
- Labeler code
- 76845
- Product ID
- 76845-101_a43c9926-5014-34bf-e053-2a95a90acdfc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Double Rider Medicine Co., Ltd.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 75 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76845-101-01 | Peppermint Aqua | 20 mL in 1 BOTTLE | LIQUID | 20 | | 1 |
| 76845-101-02 | Peppermint Aqua | 50 mL in 1 BOTTLE | LIQUID | 50 | | 1 |
| 76845-101-03 | Peppermint Aqua | 60 mL in 1 BOTTLE | LIQUID | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76845-101 | PEPPERMINT AQUA (ALCOHOL) LIQUID [DOUBLE RIDER MEDICINE CO., LTD.] | 1 | Legacy NDC, 3 package rows | 20200427_a43c9926-5022-34bf-e053-2a95a90acdfc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76845-101-01 | 76845010101 | 20 mL in 1 BOTTLE (76845-101-01) | 20 ml | 2020-03-30 | 0000-00-00 | No | No | Current |
| 76845-101-02 | 76845010102 | 50 mL in 1 BOTTLE (76845-101-02) | 50 ml | 2020-03-30 | 0000-00-00 | No | No | Current |
| 76845-101-03 | 76845010103 | 60 mL in 1 BOTTLE (76845-101-03) | 60 ml | 2020-03-30 | 0000-00-00 | No | No | Current |