Koi Hand Sanitizer
- Product NDC
- 73842-003
- 11-digit product format
- 738420003
- Labeler code
- 73842
- Product ID
- 73842-003_abc0d09a-614c-cfcb-e053-2a95a90af8bd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol, 70%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Koi CBD LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-03
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 g/100mL
- 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 |
|---|
| 73842-003-01 | Koi Hand Sanitizer | 59 mL in 1 BOTTLE | GEL | 59 | | 1 |
| 73842-003-02 | Koi Hand Sanitizer | 118 mL in 1 BOTTLE | GEL | 118 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73842-003 | KOI HAND SANITIZER (ETHYL ALCOHOL, 70%) GEL [KOI CBD LLC] | 1 | Legacy NDC, 2 package rows | 20200803_abc1264b-1a0d-bec3-e053-2995a90a0df5.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 |
|---|
| 73842-003-01 | 73842000301 | 59 mL in 1 BOTTLE (73842-003-01) | 59 ml | 2020-08-03 | 0000-00-00 | No | No | Current |
| 73842-003-02 | 73842000302 | 118 mL in 1 BOTTLE (73842-003-02) | 118 ml | 2020-08-03 | 0000-00-00 | No | No | Current |