Hanzol
- Product NDC
- 76917-080
- 11-digit product format
- 769170080
- Labeler code
- 76917
- Product ID
- 76917-080_a6808b7b-ff00-42e6-a167-51e670d70859
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Plymouth Technology, Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 80 L/100L
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 76917-080-01 | Hanzol Liquid Hand Sanitizer | 3.8 L in 1 CONTAINER | LIQUID | 3.8 | | 1 |
| 76917-080-05 | Hanzol Liquid Hand Sanitizer | 18.9 L in 1 CONTAINER | LIQUID | 18.9 | | 1 |
| 76917-080-55 | Hanzol Liquid Hand Sanitizer | 208.2 L in 1 DRUM | LIQUID | 208.2 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76917-080 | HANZOL LIQUID HAND SANITIZER (ETHYL ALCOHOL) LIQUID [PLYMOUTH TECHNOLOGY, INC] | 1 | Legacy NDC, 3 package rows | 20200523_a1e0354a-d60b-49a1-9b66-a9d021156cdc.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 |
|---|
| 76917-080-01 | 76917008001 | 3.8 L in 1 CONTAINER (76917-080-01) | 3.8 l | 2020-05-01 | 0000-00-00 | No | No | Current |
| 76917-080-05 | 76917008005 | 18.9 L in 1 CONTAINER (76917-080-05) | 18.9 l | 2020-05-01 | 0000-00-00 | No | No | Current |
| 76917-080-55 | 76917008055 | 208.2 L in 1 DRUM (76917-080-55) | 208.2 l | 2020-05-01 | 0000-00-00 | No | No | Current |