Argentum Quartz
- Product NDC
- 53645-1340
- 11-digit product format
- 536451340
- Labeler code
- 53645
- Product ID
- 53645-1340_ba25ed16-eaa8-6d71-e053-2995a90abff5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Argentum Quartz
- Dosage form
- GLOBULE
- Route
- ORAL
- Labeler
- True Botanica, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-06-20
- Marketing end
- 0000-00-00
- Substance
- SILVER; SILICON DIOXIDE
- Active strength
- 6 [hp_X]/23g; [hp_X]/23g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53645-1340 | ARGENTUM QUARTZ GLOBULE [TRUE BOTANICA, LLC] | 3 | Legacy NDC | 20210131_d1c4d69e-7702-43ba-8eeb-ca65dfa53fa2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53645-1340-2 | 53645134002 | 23 g in 1 BOTTLE (53645-1340-2) | 23 g | 2013-06-20 | 0000-00-00 | No | No | Current |