OPTISOURCE Antibacterial Foam Hand
- Product NDC
- 64646-001
- 11-digit product format
- 646460001
- Labeler code
- 64646
- Product ID
- 64646-001_98dfe2f3-88e9-737e-e053-2a95a90ac37a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- Charlotte Products Ltd.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-11-03
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 64646-001-02 | OPTISOURCE Antibacterial Foam Hand | 4 in 1 CASE | SOAP | 4 | | 10 |
| 64646-001-02 | OPTISOURCE Antibacterial Foam Hand | 1250 mL in 1 BOTTLE, DISPENSING | SOAP | 1250 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64646-001 | OPTISOURCE ANTIBACTERIAL FOAM HAND (BENZALKONIUM CHLORIDE) SOAP [CHARLOTTE PRODUCTS LTD.] | 10 | Legacy NDC, 2 package rows | 20191205_20fc9143-e675-18ae-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64646-001-02 | 64646000102 | 4 in 1 CASE | Historical |