Hand Sanitizer
- Product NDC
- 78185-003
- 11-digit product format
- 781850003
- Labeler code
- 78185
- Product ID
- 78185-003_a85690a1-42ab-98ce-e053-2a95a90a5bc8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYL ALCOHOL 70%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Sun Hing Foods Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 80 mL/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 |
|---|
| 78185-003-01 | Hand Sanitizer | 888 mL in 1 BOTTLE, PLASTIC | GEL | 888 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 78185-003 | HAND SANITIZER (ETHYL ALCOHOL 70%) GEL [SUN HING FOODS INC] | 5 | Legacy NDC, 1 package rows | 20200618_a85690a1-42b9-98ce-e053-2a95a90a5bc8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 78185-003-01 | 78185000301 | 888 mL in 1 BOTTLE, PLASTIC | 888 ml | Historical |