Ancos Silver Ion Hand Sanitizer
- Product NDC
- 75139-006
- 11-digit product format
- 751390006
- Labeler code
- 75139
- Product ID
- 75139-006_adab9831-3a85-16fc-e053-2a95a90a1c81
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ancos Silver Ion Hand Sanitizer
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Anson Bio-Technology Co., Ltd.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-04-28
- Marketing end
- 0000-00-00
- Substance
- SILVER CATION; ALCOHOL
- Active strength
- 0 g/100mL; mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 75139-006-01 | Ancos Silver Ion Hand Sanitizer | 100 mL in 1 BOTTLE | GEL | 100 | | 2 |
| 75139-006-02 | Ancos Silver Ion Hand Sanitizer | 500 mL in 1 BOTTLE | GEL | 500 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75139-006 | ANCOS SILVER ION HAND SANITIZER GEL [ANSON BIO-TECHNOLOGY CO., LTD.] | 2 | Legacy NDC, 2 package rows | 20200825_a454c956-b711-2e95-e053-2a95a90a9fda.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 75139-006-01 | 75139000601 | 100 mL in 1 BOTTLE (75139-006-01) | 100 ml | 2020-04-28 | 0000-00-00 | No | No | Current |
| 75139-006-02 | 75139000602 | 500 mL in 1 BOTTLE (75139-006-02) | 500 ml | 2020-04-28 | 0000-00-00 | No | No | Current |