Maxim Instant Foam Hand Sanitizer
- Product NDC
- 70542-250
- 11-digit product format
- 705420250
- Labeler code
- 70542
- Product ID
- 70542-250_cb03703e-853f-2912-e053-2a95a90a1474
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Midlab, Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-10-21
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70542-250-32 | 70542025032 | 443 mL in 1 BOTTLE, PLASTIC (70542-250-32) | 443 ml | 2021-10-21 | 0000-00-00 | No | No | Current |
| 70542-250-41 | 70542025041 | 3785 mL in 1 BOTTLE, PLASTIC (70542-250-41) | 3785 ml | 2021-10-21 | 0000-00-00 | No | No | Current |
| 70542-250-55 | 70542025055 | 208198 mL in 1 DRUM (70542-250-55) | 208198 ml | 2021-10-21 | 0000-00-00 | No | No | Current |