Cold Sore Treatment
- Product NDC
- 50730-2001
- 11-digit product format
- 507302001
- Labeler code
- 50730
- Product ID
- 50730-2001_d4aa6122-d5aa-4144-b45e-cbeaa358e738
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- TINCTURE
- Route
- TOPICAL
- Labeler
- H and P Industries, Inc. dba Triad Group
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2007-06-01
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 mL/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 50730-2001-1 | Cold Sore Treatment | 1 in 1 PACKAGE | TINCTURE | 1 | | 1 |
| 50730-2001-1 | Cold Sore Treatment | 0.6 mL in 1 VIAL, PATENT DELIVERY SYSTEM | TINCTURE | 0.6 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50730-2001 | COLD SORE TREATMENT (BENZALKONIUM CHLORIDE) TINCTURE [H AND P INDUSTRIES, INC. DBA TRIAD GROUP] | 1 | Legacy NDC, 2 package rows | 20091211_b5dee7a2-29d2-4d82-9d27-0c9a50661aca.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50730-2001-1 | 50730200101 | 1 in 1 PACKAGE | Historical |