Amethyst Rosa
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2018-04-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:00:13
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Take 3-4 times daily. Ages 12 and older: 1-2 capsules. Ages 2-11: 1 capsule. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Amethyst (Nat. silicic acid anhydrate with traces of manganese and iron) 2X, Carbo betulae (Birch wood charcoal) 2X, Fumaria (Fumitory) 3X, Absinthium (Wormwood) 4X, Betula (Borage) 4X, Calamus (Sweet flag) 4X, Chamomilla (Chamomile) 4X, Cochlearia (Common scurvy grass) 4X, Gentiana (Yellow gentian) 4X, Geum urbanum (Herb bennet) 4X, Oxalis (Wood sorrel) 4X, Rosa (Garden rose) 4X, Urtica dioica (Stinging nettle) 4X, Urtica dioica (Stinging nettle) 4X, Zingiberis (Ginger) 4X, Antimonite (Nat. antimony trisulfide) 5X, Piper nigrum (Black pepper) 5X, Hematite (Red iron ore) 6X, Graphite (Foliated crystalline carbon) 17X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Vegetable capsules, Diatomaceous earth, Distilled water, Rose petal extract, Anise oil, Caraway oil
OTC - PURPOSE SECTION
Use: Temporary relief of acne.
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. Do not use if allergic to any ingredient. 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 Made with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ACORUS CALAMUS ROOT | ACTIVE INGREDIENT | XY1K7KIQ0F | 1 | |
| ACTIVATED CHARCOAL | ACTIVE INGREDIENT | 2P3VWU3H10 | 1 | |
| ANTIMONY TRISULFIDE | ACTIVE INGREDIENT | F79059A38U | 1 | |
| BETULA PUBESCENS LEAF | ACTIVE INGREDIENT | 84SOH0O3OO | 1 | |
| BLACK PEPPER | ACTIVE INGREDIENT | KM66971LVF | 1 | |
| COCHLEARIA OFFICINALIS FLOWERING TOP | ACTIVE INGREDIENT | M87UN67CKR | 1 | |
| FERRIC OXIDE RED | ACTIVE INGREDIENT | 1K09F3G675 | 1 | |
| FUMARIA OFFICINALIS FLOWERING TOP | ACTIVE INGREDIENT | VH659J61ZL | 1 | |
| GENTIANA LUTEA ROOT | ACTIVE INGREDIENT | S72O3284MS | 1 | |
| GEUM URBANUM ROOT | ACTIVE INGREDIENT | 33P1Z2B61F | 1 | |
| GINGER | ACTIVE INGREDIENT | C5529G5JPQ | 1 | |
| GRAPHITE | ACTIVE INGREDIENT | 4QQN74LH4O | 1 | |
| MATRICARIA RECUTITA | ACTIVE INGREDIENT | G0R4UBI2ZZ | 1 | |
| OXALIS MONTANA LEAF | ACTIVE INGREDIENT | U1W3U02EW0 | 1 | |
| ROSA RUGOSA FLOWER BUD | ACTIVE INGREDIENT | TZ0BE8I3MW | 1 | |
| SILICON DIOXIDE | ACTIVE INGREDIENT | ETJ7Z6XBU4 | 1 | |
| URTICA DIOICA LEAF | ACTIVE INGREDIENT | X6M0DRN46Q | 1 | |
| URTICA DIOICA ROOT | ACTIVE INGREDIENT | J8HE8A6E5T | 1 | |
| WORMWOOD | ACTIVE INGREDIENT | F84709P2XV | 1 | |
| ACORUS CALAMUS ROOT | ACTIVE MOIETY | XY1K7KIQ0F | 1 | |
| ACTIVATED CHARCOAL | ACTIVE MOIETY | 2P3VWU3H10 | 1 | |
| ANTIMONY TRISULFIDE | ACTIVE MOIETY | F79059A38U | 1 | |
| BETULA PUBESCENS LEAF | ACTIVE MOIETY | 84SOH0O3OO | 1 | |
| BLACK PEPPER | ACTIVE MOIETY | KM66971LVF | 1 | |
| COCHLEARIA OFFICINALIS FLOWERING TOP | ACTIVE MOIETY | M87UN67CKR | 1 | |
| COLLOIDAL SILICON DIOXIDE | ACTIVE MOIETY | ETJ7Z6XBU4 | 1 | |
| FERRIC OXIDE RED | ACTIVE MOIETY | 1K09F3G675 | 1 | |
| FUMARIA OFFICINALIS FLOWERING TOP | ACTIVE MOIETY | VH659J61ZL | 1 | |
| GENTIANA LUTEA ROOT | ACTIVE MOIETY | S72O3284MS | 1 | |
| GEUM URBANUM ROOT | ACTIVE MOIETY | 33P1Z2B61F | 1 | |
| GINGER | ACTIVE MOIETY | C5529G5JPQ | 1 | |
| GRAPHITE | ACTIVE MOIETY | 4QQN74LH4O | 1 | |
| MATRICARIA RECUTITA | ACTIVE MOIETY | G0R4UBI2ZZ | 1 | |
| OXALIS MONTANA LEAF | ACTIVE MOIETY | U1W3U02EW0 | 1 | |
| ROSA RUGOSA FLOWER BUD | ACTIVE MOIETY | TZ0BE8I3MW | 1 | |
| URTICA DIOICA LEAF | ACTIVE MOIETY | X6M0DRN46Q | 1 | |
| URTICA DIOICA ROOT | ACTIVE MOIETY | J8HE8A6E5T | 1 | |
| WORMWOOD | ACTIVE MOIETY | F84709P2XV | 1 | |
| ANISE OIL | INACTIVE INGREDIENT | 6Y89129C8H | 1 | |
| CARAWAY OIL | INACTIVE INGREDIENT | C2J9B08Q3I | 1 | |
| DIATOMACEOUS EARTH | INACTIVE INGREDIENT | 2RF6EJ0M85 | 1 | |
| POWDERED CELLULOSE | INACTIVE INGREDIENT | SMD1X3XO9M | 1 | |
| ROSA RUGOSA FLOWER | INACTIVE INGREDIENT | 969IQC5YJU | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- Amethyst Rosa
- POWDERED CELLULOSE
- DIATOMACEOUS EARTH
- WATER
- ROSA RUGOSA FLOWER
- ANISE OIL
- CARAWAY OIL
- SILICON DIOXIDE
- ACTIVATED CHARCOAL
- FUMARIA OFFICINALIS FLOWERING TOP
- WORMWOOD
- BETULA PUBESCENS LEAF
- ACORUS CALAMUS ROOT
- MATRICARIA RECUTITA
- COCHLEARIA OFFICINALIS FLOWERING TOP
- GENTIANA LUTEA ROOT
- GEUM URBANUM ROOT
- OXALIS ACETOSELLA LEAF
- ROSA RUGOSA FLOWER BUD
- URTICA DIOICA LEAF
- URTICA DIOICA ROOT
- GINGER
- ANTIMONY TRISULFIDE
- BLACK PEPPER
- FERRIC OXIDE RED
- GRAPHITE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1271 | 48951-1271-7 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | TABLET / ORAL | 1582 mg | ||
| ANISE OIL | ANISE OIL | 6Y89129C8H | PASTILLE / ORAL | 16 mg | ||
| DIATOMACEOUS EARTH | DIATOMACEOUS EARTH | 2RF6EJ0M85 | TABLET, CHEWABLE / ORAL | 2 mg | ||
| DIATOMACEOUS EARTH | DIATOMACEOUS EARTH | 2RF6EJ0M85 | CAPSULE / ORAL | 3.4 mg | ||
| ANISE OIL | ANISE OIL | 6Y89129C8H | SUSPENSION / ORAL | 1 ml/5ml | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | TABLET, DELAYED RELEASE / ORAL | 16 mg | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | PASTE, DENTIFRICE / DENTAL | NA | ||
| DIATOMACEOUS EARTH | DIATOMACEOUS EARTH | 2RF6EJ0M85 | ELIXIR / ORAL | NA | ||
| DIATOMACEOUS EARTH | DIATOMACEOUS EARTH | 2RF6EJ0M85 | TABLET / ORAL | 88 mg | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | DISC / EXTRACORPOREAL | NA | ||
| ANISE OIL | ANISE OIL | 6Y89129C8H | POWDER, DENTIFRICE / DENTAL | NA | ||
| DIATOMACEOUS EARTH | DIATOMACEOUS EARTH | 2RF6EJ0M85 | TABLET, EXTENDED RELEASE / ORAL | 5 mg | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | TABLET / BUCCAL | 4.5 mg | ||
| ANISE OIL | ANISE OIL | 6Y89129C8H | SOLUTION / ORAL | 1.4 mg | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | TABLET, CHEWABLE / ORAL | NA | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | DROPS / ORAL | NA | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | CAPSULE / ORAL | 2430 mg | ||
| DIATOMACEOUS EARTH | DIATOMACEOUS EARTH | 2RF6EJ0M85 | CONCENTRATE / ORAL | NA | ||
| DIATOMACEOUS EARTH | DIATOMACEOUS EARTH | 2RF6EJ0M85 | SOAP / TOPICAL | 0.27 %w/w | ||
| DIATOMACEOUS EARTH | DIATOMACEOUS EARTH | 2RF6EJ0M85 | CAPSULE, EXTENDED RELEASE / ORAL | 5 mg | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | LIQUID / ORAL | NA | ||
| DIATOMACEOUS EARTH | DIATOMACEOUS EARTH | 2RF6EJ0M85 | SYRUP / ORAL | NA | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | POWDER, FOR SUSPENSION / ORAL | 1600 mg | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | SUSPENSION / ORAL | 1600 mg | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | DISC / TOPICAL | NA | ||
| ANISE OIL | ANISE OIL | 6Y89129C8H | DROPS / ORAL | 0.4 mg/1ml | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | TABLET, EXTENDED RELEASE / ORAL | 156 mg | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | TABLET, FILM COATED / ORAL | 392 mg | ||
| ANISE OIL | ANISE OIL | 6Y89129C8H | ELIXIR / ORAL | 0.15 ml/5ml | ||
| ANISE OIL | ANISE OIL | 6Y89129C8H | PASTE, DENTIFRICE / DENTAL | NA | ||
| DIATOMACEOUS EARTH | DIATOMACEOUS EARTH | 2RF6EJ0M85 | TABLET, COATED / ORAL | 7.2 mg | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | TABLET, COATED / ORAL | 40.2 mg | ||
| POWDERED CELLULOSE | POWDERED CELLULOSE | SMD1X3XO9M | TABLET / SUBLINGUAL | 4.5 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 |
|---|---|---|---|---|---|---|
| 05b727aa-064c-f886-e063-6394a90a38f1 | d6a72def-ff7c-40eb-8f0a-8278e70a84e3 | 2023-09-19 | Warnings | d6a72def-ff7c-40eb-8f0a-8278e70a84e3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
