NDC 63940-002 - Instant Hand Sanitizer Convenience Pack
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 63940-002
- Package NDCs from labels
- 63940-002-01
- Manufacturer
- Harmon Stores Inc
- Effective date
- 2018-11-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Instant Hand Sanitizer Convenience Pack - Harmon Stores Inc | Harmon Stores Inc | 2018-11-08 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63940-002-01 | Instant Hand Sanitizer Convenience Pack | 30 mL in 1 BOTTLE | GEL | 90 mL | 620 mg in 1mL | 4 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ALCOHOL | ACTIVE INGREDIENT | 3K9958V90M | INSTANT HAND SANITIZER CONVENIENCE PACK (ALCOHOL) KIT [HARMON STORES INC] | 2 | |
| ALCOHOL | ACTIVE MOIETY | 3K9958V90M | INSTANT HAND SANITIZER CONVENIENCE PACK (ALCOHOL) KIT [HARMON STORES INC] | 2 | |
| ALOE VERA LEAF | INACTIVE INGREDIENT | ZY81Z83H0X | INSTANT HAND SANITIZER CONVENIENCE PACK (ALCOHOL) KIT [HARMON STORES INC] | 2 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | INSTANT HAND SANITIZER CONVENIENCE PACK (ALCOHOL) KIT [HARMON STORES INC] | 2 | |
| TROLAMINE | INACTIVE INGREDIENT | 9O3K93S3TK | INSTANT HAND SANITIZER CONVENIENCE PACK (ALCOHOL) KIT [HARMON STORES INC] | 2 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | INSTANT HAND SANITIZER CONVENIENCE PACK (ALCOHOL) KIT [HARMON STORES INC] | 2 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.