Birch Juniper
- Product NDC
- 48951-2149
- 11-digit product format
- 489512149
- Labeler code
- 48951
- Product ID
- 48951-2149_43e13f9e-f46f-c5ad-e063-6394a90a25d7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Birch Juniper
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2021-11-03
- Substance
- BETULA PENDULA BARK; JUNIPER BERRY
- Active strength
- 1; 1 [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Birch Juniper
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BETULA PENDULA BARK | 1 [hp_X]/mL |
| JUNIPER BERRY | 1 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 40S83Y133C, O84B5194RL |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-2149-9 | Birch Juniper | 240 mL in 1 BOTTLE, GLASS | LIQUID | 240 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-2149 | BIRCH JUNIPER LIQUID [URIEL PHARMACY INC] | 4 | Current NDC, 1 package rows | 20241121_0fa00042-b326-6d2d-e063-6394a90a236d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-2149-9 | 48951214909 | 240 mL in 1 BOTTLE, GLASS (48951-2149-9) | 240 ml | 2021-11-03 | No | No | Current |