Peridot
- Product NDC
- 63083-8136
- 11-digit product format
- 630838136
- Labeler code
- 63083
- Product ID
- 63083-8136_5c5bfb28-a759-477e-a706-82e4f71396c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Peridot
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Marketing end
- 0000-00-00
- Substance
- OLIVINE
- Active strength
- 6 [hp_X]/59mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-8136 | PERIDOT 8136 (PERIDOT) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Legacy NDC | 20220218_2b60e381-28c2-4587-b982-98d6b63dacbb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-8136-2 | 63083813602 | 59 mL in 1 BOTTLE, DROPPER (63083-8136-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |