Trival
- Manufacturer
- TE-Point Doo
- Effective date
- 2009-12-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 02:02:50
Label at a glance#
ProductTrival
Active ingredientUrtica Urens, Olea Europaea Flower, St. John's Wort, Fragaria Vesca Fruit, Garlic, Fagus Sylvatica Nut
Label structure2 sections
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DESCRIPTION SECTION

Distributed By:
TRIVAL LLC
44598 Bayview Ave #12311
Clinton Twp., MI 48038
Lot Number:
Manufactured By:
TE-Point Doo
Tetovo, Macedonia
Made in Macedonia
Expiration Date:
OTC - ACTIVE INGREDIENT SECTION
Drug Facts
Active Ingredients Purpose
Dwarf Nettle (urtica urens) 1C HPUS . . . . . . . . . . . Stimulates hair growth
European beech nut (fagus sylvatica) 1C HPUS . . . Stimulates hair growth
Garlic (allium sativum) 1C HPUS . . . . . . . . . . . . . . Disinfection
Olive flower (olea europaea flos) 1C HPUS . . . . . . . Disinfection
St. John's Wort (hypericum perforatum) 2C HPUS . . Disinfection
Woodland strawberry (fragaria vesca) 1C HPUS . . . Stimulates hair growth
The letters 'HPUS' indicate that these ingredients are officially included in the Homeopathic Pharmacopeia of the United States.
Active Ingredients Purpose
Dwarf Nettle (urtica urens) 1C HPUS . . . . . . . . . . . Stimulates hair growth
European beech nut (fagus sylvatica) 1C HPUS . . . Stimulates hair growth
Garlic (allium sativum) 1C HPUS . . . . . . . . . . . . . . Disinfection
Olive flower (olea europaea flos) 1C HPUS . . . . . . . Disinfection
St. John's Wort (hypericum perforatum) 2C HPUS . . Disinfection
Woodland strawberry (fragaria vesca) 1C HPUS . . . Stimulates hair growth
The letters 'HPUS' indicate that these ingredients are officially included in the Homeopathic Pharmacopeia of the United States.
INDICATIONS & USAGE SECTION
Uses
Treats hair loss (alopecia areata) on the scalp, beard, and eyebrows.
Relieves scalp from redness, itching and dandruff.
To be used according to standard Homeopathic conditions.
Treats hair loss (alopecia areata) on the scalp, beard, and eyebrows.
Relieves scalp from redness, itching and dandruff.
To be used according to standard Homeopathic conditions.
GENERAL PRECAUTIONS SECTION
Warnings
For external use only
If pregnant or breast feeding, ask a health professional before use.
Keep out of reach of children.
Before using, ask your doctor: If you have any known allergies to the ingredients in this product; if you have had or will be having any medical condition(s) and/or procedure(s) relating to skin or scalp.
Avoid getting into eyes. If contact occurs, rinse with flowing water.
For external use only
If pregnant or breast feeding, ask a health professional before use.
Keep out of reach of children.
Before using, ask your doctor: If you have any known allergies to the ingredients in this product; if you have had or will be having any medical condition(s) and/or procedure(s) relating to skin or scalp.
Avoid getting into eyes. If contact occurs, rinse with flowing water.
OTC - WHEN USING SECTION
When using this product you may experience mild itching sensation.
DOSAGE & ADMINISTRATION SECTION
Directions
Only to be used by adults and children 12 years and older
Apply at night before bed
Pour sufficient amount into hands to cover entire scalp
Massage into scalp with hands
Rinse the next morning
Repeat procedure over the next two consecutive nights
Wait 10-15 days to see results
If no results, wait 30 days before next application
See insert for more detailed instructions
Only to be used by adults and children 12 years and older
Apply at night before bed
Pour sufficient amount into hands to cover entire scalp
Massage into scalp with hands
Rinse the next morning
Repeat procedure over the next two consecutive nights
Wait 10-15 days to see results
If no results, wait 30 days before next application
See insert for more detailed instructions
SAFE HANDLING WARNING SECTION
Other information
Store product in a cool, dry place.
Do not use product if seal has been broken
Contains 2.5% alcohol
Store product in a cool, dry place.
Do not use product if seal has been broken
Contains 2.5% alcohol
INACTIVE INGREDIENT SECTION
Inactive Ingredients
Alcohol, Blackberry
Alcohol, Blackberry
OTC - QUESTIONS SECTION
Questions?
Or to Report Adverse Events, call: TEL: 1-800-897-9830
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49998-332-16 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-c50a-621f-e053-dbdaa90a74ad | 57dff8c6-bf28-4ca3-85fa-be017afd3e84 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49998-332-16 | Trival | 1 in 1 BOX | TINCTURE | 1 | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Fagus Sylvatica Nut | ACTIVE INGREDIENT | I57ERU2601 | 3 | |
| Fragaria Vesca Fruit | ACTIVE INGREDIENT | CG6IX3GCMU | 3 | |
| Garlic | ACTIVE INGREDIENT | V1V998DC17 | 3 | |
| Olea Europaea Flower | ACTIVE INGREDIENT | 498M34P1VZ | 3 | |
| St. John's Wort | ACTIVE INGREDIENT | UFH8805FKA | 3 | |
| Urtica Urens | ACTIVE INGREDIENT | IHN2NQ5OF9 | 3 | |
| Fagus Sylvatica Nut | ACTIVE MOIETY | I57ERU2601 | 3 | |
| Fragaria Vesca Fruit | ACTIVE MOIETY | CG6IX3GCMU | 3 | |
| Garlic | ACTIVE MOIETY | V1V998DC17 | 3 | |
| Olea Europaea Flower | ACTIVE MOIETY | 498M34P1VZ | 3 | |
| St. John's Wort | ACTIVE MOIETY | UFH8805FKA | 3 | |
| Urtica Urens | ACTIVE MOIETY | IHN2NQ5OF9 | 3 | |
| Alcohol | INACTIVE INGREDIENT | 3K9958V90M | 3 | |
| Blackberry | INACTIVE INGREDIENT | 8A6OMU3I8L | 3 |
Products#
Every source-derived product name is available through these pages.
- Trival
- Homeopathic Alopecia Areata Treatment
- Urtica Urens
- Olea Europaea Flower
- St. John's Wort
- Fragaria Vesca Fruit
- Garlic
- Blackberry
- Fagus Sylvatica Nut
- Alcohol
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49998-332 | 49998-332-16 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Urtica Urens | IHN2NQ5OF9 | ACTIB |
| Olea Europaea Flower | 498M34P1VZ | ACTIB |
| St. John's Wort | UFH8805FKA | ACTIB |
| Fragaria Vesca Fruit | CG6IX3GCMU | ACTIB |
| Garlic | V1V998DC17 | ACTIB |
| Blackberry | 8A6OMU3I8L | IACT |
| Fagus Sylvatica Nut | I57ERU2601 | ACTIB |
| Alcohol | 3K9958V90M | IACT |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| Alcohol | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 462cee25-b508-4d40-9b67-acd87bb3a3d1 | 57dff8c6-bf28-4ca3-85fa-be017afd3e84 | 2009-12-22 | 462cee25-b508-4d40-9b67-acd87bb3a3d1 57dff8c6-bf28-4ca3-85fa-be017afd3e84 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
