Naturasil
- Product NDC
- 10893-630
- Requested package NDC
- 10893-630-04
- 11-digit product format
- 108930630
- Labeler code
- 10893
- Product ID
- 10893-630_2f38c66c-fbc6-4af2-b427-65c23cad47ce
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sulfur and Thuja Occidentalis
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- Nature's Innovation, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-01-13
- Marketing end
- 0000-00-00
- Substance
- SULFUR; THUJA OCCIDENTALIS LEAFY TWIG
- Active strength
- 1 [hp_X]/127.6g; [hp_X]/127.6g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 package | package | 10893-630 | 10893-630-04 | D | Discontinued by firm | 2026-10-20 |
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 | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 10893-630 | 10893-630-04 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 10893-630 | 10893-630-04 | D | Discontinued by firm | excluded / ndc_excluded.zip | f5e01cc5f278… | a2eaf40c39c3… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 10893-630-04 | 10893063004 | 113.3 g in 1 PACKAGE (10893-630-04) | 113.3 g | 2019-01-01 | 0000-00-00 | No | No | Current |