Derma-San
- Product NDC
- 63131-0006
- 11-digit product format
- 631310006
- Labeler code
- 63131
- Product ID
- 63131-0006_a49c41fd-e31e-b451-e053-2995a90a0dc6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Anderson Chemical Company
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2008-05-20
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- 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 |
|---|
| 63131-0006-1 | Derma-San | 3785 mL in 1 JUG | LIQUID | 3785 | | 1 |
| 63131-0006-1 | Derma-San | 7570 in 1 CASE | LIQUID | 7570 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63131-0006 | DERMA-SAN (BENZALKONIUM CHLORIDE) LIQUID [ANDERSON CHEMICAL COMPANY] | 1 | Legacy NDC, 2 package rows | 20200506_a49c41fd-e31d-b451-e053-2995a90a0dc6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63131-0006-1 | 63131000601 | 7570 JUG in 1 CASE (63131-0006-1) > 3785 mL in 1 JUG | 7570 jug | 2008-05-20 | 0000-00-00 | No | No | Current |