Simpurity Hand Sanitizer
- Product NDC
- 74069-002
- 11-digit product format
- 740690002
- Labeler code
- 74069
- Product ID
- 74069-002_d397dd80-2ee8-e490-e053-2a95a90a9e83
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Truesdell Manufacturing & Consulting, LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-04
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 75 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 74069-002-04 | Simpurity Hand Sanitizer | 120 mL in 1 BOTTLE, GLASS | GEL | 120 | | 3 |
| 74069-002-08 | Simpurity Hand Sanitizer | 240 mL in 1 BOTTLE, GLASS | GEL | 240 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 74069-002 | SIMPURITY HAND SANITIZER (ALCOHOL) GEL [TRUESDELL MANUFACTURING & CONSULTING, LLC] | 3 | Legacy NDC, 2 package rows | 20211221_a47cf893-4ec1-6e8d-e053-2a95a90a4cf5.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 |
|---|
| 74069-002-04 | 74069000204 | 120 mL in 1 BOTTLE, GLASS (74069-002-04) | 120 ml | 2020-05-04 | 0000-00-00 | No | No | Current |
| 74069-002-08 | 74069000208 | 240 mL in 1 BOTTLE, GLASS (74069-002-08) | 240 ml | 2020-05-04 | 0000-00-00 | No | No | Current |