KYOSILK
- Product NDC
- 73353-0001
- 11-digit product format
- 733530001
- Labeler code
- 73353
- Product ID
- 73353-0001_92a365f4-7c6a-625e-e053-2995a90ad49c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- silk sheet, hydrogen water
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- TOYOWADO SILKTECH CO., LTD
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-09-14
- Marketing end
- 0000-00-00
- Substance
- SILK SERICIN
- Active strength
- 40 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 73353-0001-1 | KYOSILK | 30 mL in 1 PACKAGE | LIQUID | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73353-0001 | KYOSILK (SILK SHEET, HYDROGEN WATER) LIQUID [TOYOWADO SILKTECH CO., LTD] | 2 | Legacy NDC, 1 package rows | 20190916_927ef0e2-a74b-54a5-e053-2995a90aa262.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 73353-0001-1 | 73353000101 | 30 mL in 1 PACKAGE | 30 ml | Historical |