Sulfur Facial Wash
- Product NDC
- 68437-012
- 11-digit product format
- 684370012
- Labeler code
- 68437
- Product ID
- 68437-012_eb0475c6-c75a-55a1-e053-2a95a90a69e9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sulfur
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- GRISI Hnos, S.A DE C.V
- Application
- M006
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-07-08
- Marketing end
- 0000-00-00
- Substance
- SULFUR
- Active strength
- 3 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 | 68437-012 | D | Discontinued by firm | 2026-10-12 | ||
| excluded package | package | 68437-012 | 68437-012-84 | D | Discontinued by firm | 2026-10-12 |
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.
| Captured / source date | Dataset | Scope | Package NDC | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | D | Discontinued by firm | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 68437-012-84 | D | Discontinued by firm | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | D | Discontinued by firm | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 68437-012-84 | D | Discontinued by firm | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 68437-012-84 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68437-012-84 | 68437001284 | 250 mL in 1 BOTTLE, PLASTIC (68437-012-84) | 250 ml | 2019-07-08 | 0000-00-00 | No | No | Current |