MEDIBLUE
- Product NDC
- 76847-301
- 11-digit product format
- 768470301
- Labeler code
- 76847
- Product ID
- 76847-301_d854902c-1fa3-5cd8-e053-2995a90a4014
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HYPOCHLOROUS ACID
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Multibio Co., Ltd
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-06-27
- Marketing end
- 0000-00-00
- Substance
- HYPOCHLOROUS ACID
- Active strength
- 0 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 |
|---|
| 76847-301-01 | MEDIBLUE | 500 mL in 1 BOTTLE, SPRAY | LIQUID | 500 | | 2 |
| 76847-301-02 | MEDIBLUE | 4000 mL in 1 BOTTLE | LIQUID | 4000 | | 2 |
| 76847-301-03 | MEDIBLUE | 20000 mL in 1 BOTTLE | LIQUID | 20000 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76847-301 | MEDIBLUE (HYPOCHLOROUS ACID) LIQUID [MULTIBIO CO., LTD] | 2 | Legacy NDC, 3 package rows | 20220219_a90af147-2f20-32c9-e053-2995a90ac5b1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76847-301-01 | 76847030101 | 500 mL in 1 BOTTLE, SPRAY (76847-301-01) | 500 ml | 2020-06-27 | 0000-00-00 | No | No | Current |
| 76847-301-02 | 76847030102 | 4000 mL in 1 BOTTLE (76847-301-02) | 4000 ml | 2020-06-27 | 0000-00-00 | No | No | Current |
| 76847-301-03 | 76847030103 | 20000 mL in 1 BOTTLE (76847-301-03) | 20000 ml | 2020-06-27 | 0000-00-00 | No | No | Current |