RemeVerse Instant Foam Hand Sanitizer
- Product NDC
- 70317-145
- 11-digit product format
- 703170145
- Labeler code
- 70317
- Product ID
- 70317-145_f1ffbc60-13c5-2b82-e053-2995a90a9111
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- RemeVerse
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-31
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/300mL
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70317-145-30 | RemeVerse Instant Foam Hand Sanitizer | 300 mL in 1 BOTTLE, DISPENSING | LIQUID | 300 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70317-145 | REMEVERSE INSTANT FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [REMEVERSE] | 6 | Legacy NDC, 1 package rows | 20241218_a11299ca-3e05-f3cb-e053-2995a90a92e2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70317-145-04 | 70317014504 | 120 mL in 1 BOTTLE, DISPENSING (70317-145-04) | 120 ml | 2020-03-31 | 0000-00-00 | No | No | Current |
| 70317-145-30 | 70317014530 | 300 mL in 1 BOTTLE, DISPENSING (70317-145-30) | 300 ml | 2020-03-31 | 0000-00-00 | No | No | Current |