Opal 30
- Product NDC
- 48951-7112
- 11-digit product format
- 489517112
- Labeler code
- 48951
- Product ID
- 48951-7112_6d583776-5ee6-f54f-e053-2991aa0aa6e4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Opal 30
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- HYDRATED SILICA
- Active strength
- 30 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| Y6O7T4G8P9 | HYDRATED SILICA | 1343-98-2 | HYDRATED SILICA |