Royal Non-Alcohol Foam Hand Sanitizer
- Product NDC
- 70415-205
- 11-digit product format
- 704150205
- Labeler code
- 70415
- Product ID
- 70415-205_d4b849f0-b187-6443-e053-2a95a90a895b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- CWGC LA Inc.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-03-22
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70415-205-01 | Royal Non-Alcohol Foam Hand Sanitizer | 1000 mL in 1 BOTTLE | SOLUTION | 1000 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70415-205 | ROYAL NON-ALCOHOL FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [CWGC LA INC.] | 12 | Legacy NDC, 1 package rows | 20231214_05364f49-c8a9-41a3-a536-9cc2f53bb884.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 |
|---|
| 70415-205-01 | 70415020501 | 1000 mL in 1 BOTTLE (70415-205-01) | 1000 ml | 2017-03-22 | 0000-00-00 | No | No | Current |