Hand wash
- Product NDC
- 52578-001
- 11-digit product format
- 525780001
- Labeler code
- 52578
- Product ID
- 52578-001_d87f9ded-2f52-ecec-e053-2995a90a2b4f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hand wash
- Dosage form
- LIQUID
- Route
- EXTRACORPOREAL
- Labeler
- FUJIAN BLUE-TOUCH PRODUCTS INC.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-05-11
- Marketing end
- 0000-00-00
- Substance
- SODIUM LAURETH SULFATE
- Active strength
- 33 g/300mL
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52578-001-01 | Hand wash | 300 mL in 1 BOTTLE | LIQUID | 300 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52578-001 | HAND WASH LIQUID [FUJIAN BLUE-TOUCH PRODUCTS INC.] | 4 | Legacy NDC, 1 package rows | 20220221_a55ba232-8cc7-7e10-e053-2995a90afdb6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52578-001-01 | 52578000101 | 300 mL in 1 BOTTLE (52578-001-01) | 300 ml | 2020-05-11 | 0000-00-00 | No | No | Current |