Foaming Hand
- Product NDC
- 82110-001
- 11-digit product format
- 821100001
- Labeler code
- 82110
- Product ID
- 82110-001_d96a8bc3-888a-4f53-e053-2a95a90a3e68
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- SHIBY INC
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-06-27
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 82110-001-01 | Foaming Hand | 3780 mL in 1 BOTTLE | LIQUID | 3780 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82110-001 | FOAMING HAND (BENZALKONIUM CHLORIDE) LIQUID [SHIBY INC] | 3 | Legacy NDC, 1 package rows | 20230224_c936af2b-4997-d6da-e053-2995a90aa066.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 |
|---|
| 82110-001-01 | 82110000101 | 3780 mL in 1 BOTTLE (82110-001-01) | 3780 ml | 2021-06-27 | 0000-00-00 | No | No | Current |