Juniperus Eucalyptus
- Product NDC
- 48951-6003
- 11-digit product format
- 489516003
- Labeler code
- 48951
- Product ID
- 48951-6003_7caee54c-a45a-cfd5-e053-2a91aa0ae020
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Juniperus Eucalyptus
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- BERBERIS VULGARIS ROOT BARK; ACORUS CALAMUS ROOT; CAMPHOR (NATURAL); C12-17 ALKANE; LARIX DECIDUA RESIN; SOLIDAGO CANADENSIS FLOWERING TOP
- Active strength
- 1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-6003-7 | 48951600307 | 90 CAPSULE, LIQUID FILLED in 1 BOTTLE, GLASS (48951-6003-7) | 2009-09-01 | 0000-00-00 | No | No | Current |