Merthiolate
- Product NDC
- 0395-9122
- 11-digit product format
- 003959122
- Labeler code
- 0395
- Product ID
- 0395-9122_a885346e-a8e7-c83e-e053-2a95a90aa083
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Humco Holding Group, Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1998-03-25
- 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 |
|---|
| 0395-9122-92 | Merthiolate | 59 mL in 1 BOTTLE | LIQUID | 59 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0395-9122 | MERTHIOLATE (BENZALKONIUM CHLORIDE) LIQUID [HUMCO HOLDING GROUP, INC.] | 3 | Legacy NDC, 1 package rows | 20200622_60645c63-bb74-49ea-e053-2a91aa0aeea6.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 |
|---|
| 0395-9122-92 | 00395912292 | 59 mL in 1 BOTTLE (0395-9122-92) | 59 ml | 2017-11-14 | 0000-00-00 | No | No | Current |