SUCROSE
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2018-05-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:59:05
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Equisetum (Common horsetail) 2X, Levisticum (Lovage) 2X, Prunus spin. (Blackthorn) 2X, Urtica dioica (Stinging nettle) 2X, Filix (Male fern) 3X, Formica (Red wood ant) 3X, Pteridium (Eagle fern) 3X, Scolopendrium (Hart's tongue) 3X, Gland. thymus (Bovine thymus) 4X, Hepar (Bovine liver) 4X, Conchae (Oyster shells) 5X, Argentum met. (Silver) 6X, Renes (Bovine kidneys) 6X, Thuja (American arborvitae) 6X, Agaricus (Fly agaric mushroom) 7X, Quartz (Rock crystal) 12X, Mercurius vivus (Mercury) 14X, Carbo betula (Birch wood charcoal) 20X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Sucrose, Lactose
OTC - PURPOSE SECTION
Use: Temporary relief of headache.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN.
WARNINGS SECTION
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| AMANITA MUSCARIA FRUITING BODY | ACTIVE INGREDIENT | DIF093I037 | 1 | |
| ASPLENIUM SCOLOPENDRIUM TOP | ACTIVE INGREDIENT | HJA3YWQ7HL | 1 | |
| BOS TAURUS THYMUS | ACTIVE INGREDIENT | 8XEJ88V2T8 | 1 | |
| COLLOIDAL SILICON DIOXIDE | ACTIVE INGREDIENT | ETJ7Z6XBU4 | 1 | |
| DRYOPTERIS FILIX-MAS ROOT | ACTIVE INGREDIENT | C0ZK0RRF5X | 1 | |
| EQUISETUM ARVENSE TOP | ACTIVE INGREDIENT | 1DP6Y6B65Z | 1 | |
| FORMICA RUFA | ACTIVE INGREDIENT | 55H0W83JO5 | 1 | |
| LEVISTICUM OFFICINALE ROOT | ACTIVE INGREDIENT | 46QZ19OEX8 | 1 | |
| MAMMAL LIVER | ACTIVE INGREDIENT | D0846624BI | 1 | |
| MERCURY | ACTIVE INGREDIENT | FXS1BY2PGL | 1 | |
| OSTREA EDULIS SHELL | ACTIVE INGREDIENT | 49OY13BE7Z | 1 | |
| PORK KIDNEY | ACTIVE INGREDIENT | X7BCI5P86H | 1 | |
| PTERIDIUM AQUILINUM WHOLE | ACTIVE INGREDIENT | 05T3M06HCM | 1 | |
| SILVER | ACTIVE INGREDIENT | 3M4G523W1G | 1 | |
| SLOE | ACTIVE INGREDIENT | 3MLB4858X7 | 1 | |
| THUJA OCCIDENTALIS WHOLE | ACTIVE INGREDIENT | 5HBV6WCE3N | 1 | |
| URTICA DIOICA | ACTIVE INGREDIENT | 710FLW4U46 | 1 | |
| AMANITA MUSCARIA FRUITING BODY | ACTIVE MOIETY | DIF093I037 | 1 | |
| ASPLENIUM SCOLOPENDRIUM TOP | ACTIVE MOIETY | HJA3YWQ7HL | 1 | |
| BOS TAURUS THYMUS | ACTIVE MOIETY | 8XEJ88V2T8 | 1 | |
| COLLOIDAL SILICON DIOXIDE | ACTIVE MOIETY | ETJ7Z6XBU4 | 1 | |
| DRYOPTERIS FILIX-MAS ROOT | ACTIVE MOIETY | C0ZK0RRF5X | 1 | |
| EQUISETUM ARVENSE TOP | ACTIVE MOIETY | 1DP6Y6B65Z | 1 | |
| FORMICA RUFA | ACTIVE MOIETY | 55H0W83JO5 | 1 | |
| LEVISTICUM OFFICINALE ROOT | ACTIVE MOIETY | 46QZ19OEX8 | 1 | |
| MAMMAL LIVER | ACTIVE MOIETY | D0846624BI | 1 | |
| MERCURY | ACTIVE MOIETY | FXS1BY2PGL | 1 | |
| OSTREA EDULIS SHELL | ACTIVE MOIETY | 49OY13BE7Z | 1 | |
| PORK KIDNEY | ACTIVE MOIETY | X7BCI5P86H | 1 | |
| PTERIDIUM AQUILINUM WHOLE | ACTIVE MOIETY | 05T3M06HCM | 1 | |
| SILVER | ACTIVE MOIETY | 3M4G523W1G | 1 | |
| SLOE | ACTIVE MOIETY | 3MLB4858X7 | 1 | |
| THUJA OCCIDENTALIS WHOLE | ACTIVE MOIETY | 5HBV6WCE3N | 1 | |
| URTICA DIOICA | ACTIVE MOIETY | 710FLW4U46 | 1 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | 1 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | 1 |
Products#
Every source-derived product name is available through these pages.
- Thuja Thymus comp.
- SUCROSE
- LACTOSE
- EQUISETUM ARVENSE TOP
- LEVISTICUM OFFICINALE ROOT
- SLOE
- URTICA DIOICA
- DRYOPTERIS FILIX-MAS ROOT
- FORMICA RUFA
- PTERIDIUM AQUILINUM WHOLE
- ASPLENIUM SCOLOPENDRIUM TOP
- BOS TAURUS THYMUS
- MAMMAL LIVER
- OSTREA EDULIS SHELL
- SILVER
- PORK KIDNEY
- THUJA OCCIDENTALIS WHOLE
- AMANITA MUSCARIA FRUITING BODY
- SILICON DIOXIDE
- MERCURY
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-9005 | 48951-9005-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| LACTOSE | J2B2A4N98G | IACT |
| EQUISETUM ARVENSE TOP | 1DP6Y6B65Z | ACTIB |
| LEVISTICUM OFFICINALE ROOT | 46QZ19OEX8 | ACTIB |
| SLOE | 3MLB4858X7 | ACTIB |
| URTICA DIOICA | 710FLW4U46 | ACTIB |
| DRYOPTERIS FILIX-MAS ROOT | C0ZK0RRF5X | ACTIB |
| FORMICA RUFA | 55H0W83JO5 | ACTIB |
| PTERIDIUM AQUILINUM WHOLE | 05T3M06HCM | ACTIB |
| ASPLENIUM SCOLOPENDRIUM TOP | HJA3YWQ7HL | ACTIB |
| BOS TAURUS THYMUS | 8XEJ88V2T8 | ACTIB |
| MAMMAL LIVER | D0846624BI | ACTIB |
| OSTREA EDULIS SHELL | 49OY13BE7Z | ACTIB |
| SILVER | 3M4G523W1G | ACTIB |
| PORK KIDNEY | X7BCI5P86H | ACTIB |
| THUJA OCCIDENTALIS WHOLE | 5HBV6WCE3N | ACTIB |
| AMANITA MUSCARIA FRUITING BODY | DIF093I037 | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| MERCURY | FXS1BY2PGL | ACTIB |
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 |
|---|---|---|---|---|---|---|
| SUCROSE | SUCROSE | C151H8M554 | TABLET, EXTENDED RELEASE / ORAL | 284.54 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET / RECTAL | 20 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | FILM, EXTENDED RELEASE / TRANSDERMAL | 675 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | ELIXIR / ORAL | 18000 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TROCHE / BUCCAL | NA | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CAPSULE, COATED, EXTENDED RELEASE / ORAL | NA | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS | 2000 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | SUSPENSION, EXTENDED RELEASE / ORAL | 5400 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | INJECTION / INTRAVENOUS | 203.5 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET / BUCCAL | 109 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET / SUBLINGUAL | 109 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS | 133 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | INJECTION, SOLUTION / INTRAVENOUS | 0.45 %w/v | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CAPSULE / RESPIRATORY (INHALATION) | 44.4 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, EFFERVESCENT / ORAL | 96.5 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | POWDER, FOR SOLUTION / ORAL | 38666 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CAPSULE, EXTENDED RELEASE / ORAL | 120 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | CAPSULE / ORAL | 3568 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS | 900 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION, SOLUTION / INTRAVENOUS | NA | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET, DELAYED RELEASE / ORAL | 295.33 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | POWDER / RESPIRATORY (INHALATION) | 90 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | GRANULE, FOR SUSPENSION / ORAL | 512.5 mg/5ml | ||
| SUCROSE | SUCROSE | C151H8M554 | SOLUTION / RECTAL | 35.42 %w/v | ||
| SUCROSE | SUCROSE | C151H8M554 | SUSPENSION / ORAL | 48209 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL | 18790 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | SOLUTION / ORAL | 70000 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, COATED / ORAL | 332.05 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | SYRUP / ORAL | 46400 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | SUPPOSITORY / RECTAL | NA | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET / BUCCAL | 296.7 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION / SUBCUTANEOUS | 47.75 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | CAPSULE, COATED, EXTENDED RELEASE / ORAL | 86 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | LOZENGE / TRANSMUCOSAL | 1255 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | POWDER, FOR SUSPENSION / ORAL | 40017 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | DROPS / ORAL | NA | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, EXTENDED RELEASE / ORAL | 400 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | CONCENTRATE / ORAL | 4800 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET / ORAL | 4249 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CAPSULE, DELAYED RELEASE / ORAL | 231.84 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | PASTILLE / ORAL | 426 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | CAPSULE, EXTENDED RELEASE / ORAL | 619 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CAPSULE / ORAL | 530 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | SOLUTION / RECTAL | 8 %w/v | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET, CHEWABLE / ORAL | 7258 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | CAPSULE, DELAYED RELEASE / ORAL | 955 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, SUGAR COATED / ORAL | NA | ||
| LACTOSE | LACTOSE | J2B2A4N98G | SOLUTION / ORAL | 1682 mg/15ml | ||
| SUCROSE | SUCROSE | C151H8M554 | SUSPENSION/ DROPS / ORAL | 3750 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET, FILM COATED, EXTENDED RELEASE / ORAL | 119.12 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS | 308 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | POWDER / ORAL | 27768 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | GRANULE, FOR SUSPENSION / ORAL | 31885 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | POWDER, FOR SOLUTION / ORAL | NA | ||
| SUCROSE | SUCROSE | C151H8M554 | TROCHE / ORAL | NA | ||
| SUCROSE | SUCROSE | C151H8M554 | CAPSULE, COATED PELLETS / ORAL | 59.8 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | OINTMENT / TOPICAL | NA | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET / SUBLINGUAL | 352 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CREAM / VAGINAL | 3 %w/w | ||
| LACTOSE | LACTOSE | J2B2A4N98G | SUPPOSITORY / VAGINAL | NA |
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 |
|---|---|---|---|---|---|---|
| 0f12e34a-9079-d4df-e063-6294a90ab239 | 1c10ddca-abde-49cd-a30f-d5bfd628f38c | 2024-01-16 | Warnings | 1c10ddca-abde-49cd-a30f-d5bfd628f38c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
