BIG WIPES Multi-Purpose
- Product NDC
- 79705-002
- 11-digit product format
- 797050002
- Labeler code
- 79705
- Product ID
- 79705-002_ee26f5f8-cd7f-60fb-e053-2a95a90a877a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- CLOTH
- Route
- TOPICAL
- Labeler
- Sycamore USA Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-31
- Marketing end
- 2025-10-31
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 | 79705-002 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 79705-002 | 79705-002-01 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 79705-002 | 79705-002-03 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 79705-002 | 79705-002-04 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 79705-002 | 79705-002-06 | D | Discontinued by firm | 2026-10-05 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Dataset | Scope | Package NDC |
|---|---|---|
| excluded product | product | |
| excluded package | package | 79705-002-06 |
| excluded package | package | 79705-002-04 |
| excluded package | package | 79705-002-01 |
| excluded package | package | 79705-002-03 |
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 |
|---|---|---|---|---|---|---|---|---|
| 79705-002-01 | 79705000201 | 4 mL in 1 POUCH (79705-002-01) | 4 ml | 2020-08-31 | 0000-00-00 | No | No | Current |
| 79705-002-03 | 79705000203 | 110 mL in 1 CANISTER (79705-002-03) | 110 ml | 2020-08-31 | 0000-00-00 | No | No | Current |
| 79705-002-04 | 79705000204 | 310 mL in 1 CANISTER (79705-002-04) | 310 ml | 2020-08-31 | 0000-00-00 | No | No | Current |
| 79705-002-06 | 79705000206 | 1161 mL in 1 CANISTER (79705-002-06) | 1161 ml | 2020-08-31 | 0000-00-00 | No | No | Current |