Color Element Alcohol Free Hand Sanitizer
- Product NDC
- 74934-048
- 11-digit product format
- 749340048
- Labeler code
- 74934
- Product ID
- 74934-048_af4b05d0-679c-442b-e053-2995a90a1f06
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Zhejiang iColor Biotech Co., Ltd
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-09-07
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 74934-048 | D | Discontinued by firm | 2026-10-12 | ||
| excluded package | package | 74934-048 | 74934-048-01 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 74934-048 | 74934-048-02 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 74934-048-01 | 74934004801 | 30 mL in 1 BOTTLE (74934-048-01) | 30 ml | 2020-09-07 | 0000-00-00 | No | No | Current |
| 74934-048-02 | 74934004802 | 2 mL in 1 BAG (74934-048-02) | 2 ml | 2020-09-07 | 0000-00-00 | No | No | Current |