Hoo gargle (Mouthwash)
- Product NDC
- 81840-1001
- 11-digit product format
- 818401001
- Labeler code
- 81840
- Product ID
- 81840-1001_e22b8f86-7412-6e61-e053-2995a90ae0ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- xylitol
- Dosage form
- LIQUID
- Route
- DENTAL
- Labeler
- MIKO CO LTD
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-04-20
- Marketing end
- 0000-00-00
- Substance
- XYLITOL
- Active strength
- 1 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 81840-1001-1 | Hoo gargle (Mouthwash) | 10 mL in 1 CUP | LIQUID | 10 | | 1 |
| 81840-1001-2 | Hoo gargle (Mouthwash) | 30 in 1 PACKAGE | LIQUID | 30 | | 1 |
| 81840-1001-3 | Hoo gargle (Mouthwash) | 100 in 1 PACKAGE | LIQUID | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81840-1001 | HOO GARGLE (MOUTHWASH) (XYLITOL) LIQUID [MIKO CO LTD] | 1 | Legacy NDC, 3 package rows | 20220626_e22b8f0a-0321-b7f1-e053-2995a90a1d35.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81840-1001-1 | 81840100101 | 10 mL in 1 CUP | 10 ml | | | | | Historical |
| 81840-1001-2 | 81840100102 | 30 in 1 PACKAGE | | | | | | Historical |
| 81840-1001-3 | 81840100103 | 100 PACKAGE in 1 PACKAGE (81840-1001-3) > 30 CUP in 1 PACKAGE (81840-1001-2) > 10 mL in 1 CUP (81840-1001-1) | 100 package | 2021-04-20 | 0000-00-00 | No | No | Current |