Real Relief
- Product NDC
- 71971-6030
- 11-digit product format
- 719716030
- Labeler code
- 71971
- Product ID
- 71971-6030_4064be78-c5a6-4b5f-9879-7092234c952f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allium cepa, Aralia racemosa, Arsenicum album, Cuprum metallicum, Euphrasia officinalis, Nux vomica, Sabadilla, Sticta pulmonaria
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Homeolab International (Canada) inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-01-01
- Substance
- ONION; ARALIA RACEMOSA ROOT; ARSENIC TRIOXIDE; COPPER; EUPHRASIA STRICTA; STRYCHNOS NUX-VOMICA SEED; SCHOENOCAULON OFFICINALE SEED; LOBARIA PULMONARIA
- Active strength
- 8; 8; 8; 8; 8; 8; 8; 8 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Real Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ONION | 8 [hp_X]/1 |
| ARALIA RACEMOSA ROOT | 8 [hp_X]/1 |
| ARSENIC TRIOXIDE | 8 [hp_X]/1 |
| COPPER | 8 [hp_X]/1 |
| EUPHRASIA STRICTA | 8 [hp_X]/1 |
| STRYCHNOS NUX-VOMICA SEED | 8 [hp_X]/1 |
| SCHOENOCAULON OFFICINALE SEED | 8 [hp_X]/1 |
| LOBARIA PULMONARIA | 8 [hp_X]/1 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71971-6030-0 | Real Relief | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
| 71971-6030-0 | Real Relief | 1 in 1 CARTON | TABLET | 1 | | 1 |
| 71971-6030-5 | Real Relief | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 71971-6030-8 | Real Relief | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 71971-6030-8 | Real Relief | 1 in 1 CARTON | TABLET | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71971-6030 | REAL RELIEF (ALLIUM CEPA, ARALIA RACEMOSA, ARSENICUM ALBUM, CUPRUM METALLICUM, EUPHRASIA OFFICINALIS, NUX VOMICA, SABADILLA, STICTA PULMONARIA) TABLET [HOMEOLAB INTERNATIONAL (CANADA) INC] | 1 | Current NDC, Legacy NDC, 5 package rows | 20200122_d2459cd9-12e0-4ee4-950a-05d78023c89b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71971-6030-0 | 71971603000 | 1 BOTTLE in 1 CARTON (71971-6030-0) / 90 TABLET in 1 BOTTLE | 1 bottle | 2020-01-01 | 0000-00-00 | No | No | Current |
| 71971-6030-5 | 71971603005 | 30 TABLET in 1 BOTTLE (71971-6030-5) | 30 tablet | 2020-01-01 | 0000-00-00 | No | No | Current |
| 71971-6030-8 | 71971603008 | 1 BOTTLE in 1 CARTON (71971-6030-8) / 60 TABLET in 1 BOTTLE | 1 bottle | 2020-01-01 | 0000-00-00 | No | No | Current |