ARTEMIS Alcohol-Free Antiseptic Foam Hand Sanitizer
- Product NDC
- 49765-310
- 11-digit product format
- 497650310
- Labeler code
- 49765
- Product ID
- 49765-310_aa185f08-6b25-6aaa-e053-2a95a90a2db1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Artemis Bio-Solutions, Inc.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2011-02-24
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 49765-310-01 | ARTEMIS Alcohol-Free Antiseptic Foam Hand Sanitizer | 50 mL in 1 BOTTLE | LIQUID | 50 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49765-310 | ARTEMIS ALCOHOL-FREE ANTISEPTIC FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [ARTEMIS BIO-SOLUTIONS, INC.] | 4 | Legacy NDC, 1 package rows | 20200711_be8ab2b6-5581-4792-8fcd-bbbf98b52c5c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49765-310-01 | 49765031001 | 50 mL in 1 BOTTLE (49765-310-01) | 50 ml | 2011-02-24 | 0000-00-00 | No | No | Current |