Suppress Hand Sanitizer
- Product NDC
- 74913-610
- 11-digit product format
- 749130610
- Labeler code
- 74913
- Product ID
- 74913-610_ac464530-3660-e82c-e053-2a95a90ac976
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-04-08
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 75 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 |
|---|
| 74913-610-01 | Suppress Hand Sanitizer | 500 mL in 1 BOTTLE, PLASTIC | GEL | 500 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 74913-610 | SUPPRESS HAND SANITIZER (ALCOHOL) GEL [SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD] | 7 | Legacy NDC, 1 package rows | 20200807_ac464530-365f-e82c-e053-2a95a90ac976.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 |
|---|
| 74913-610-01 | 74913061001 | 500 mL in 1 BOTTLE, PLASTIC (74913-610-01) | 500 ml | 2020-04-08 | 0000-00-00 | No | No | Current |