Kalium aceticum comp 6
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2024-01-12
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:25:38
Label at a glance#
ProductKalium aceticum comp 6
Active ingredientSAFFRON, POTASSIUM ACETATE, ANTIMONY TRISULFIDE, CORALLIUM RUBRUM EXOSKELETON
Label structure9 sections
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 Ingredient: Antimonite (Nat. antimony trisulfide) 6X, Corallium rubrum (Red coral) 6X, Crocus sativa (Saffron) 6X, Kalium aceticum (Potassium acetate) 6X
INACTIVE INGREDIENT SECTION
Inactive Ingredient: Organic sucrose
"prepared using rhythmical processes"
OTC - PURPOSE SECTION
Use: Temporary relief of skin rash.
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. Contains traces of lactose. 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
Uriel, East Troy, WI 53120
shopuriel.com Lot:
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 48951-6079-2 | 2026-01-29 | C162847 | 48780-1 | 49896155-a5ac-586f-e063-e6dba90add90 | Kalium aceticum comp 6X |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-6079-2 | Kalium aceticum comp 6 | 1350 in 1 BOTTLE, GLASS | PELLET | 1350 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-6079 | KALIUM ACETICUM COMP 6 PELLET [URIEL PHARMACY INC.] | 2 | Legacy NDC, 1 package rows | 20240113_c9edf485-e2eb-1605-e053-2a95a90aff2d.zip |
Products#
Every source-derived product name is available through these pages.
- Kalium aceticum comp 6
- SAFFRON
- POTASSIUM ACETATE
- POTASSIUM CATION
- SUCROSE
- ANTIMONY TRISULFIDE
- CORALLIUM RUBRUM EXOSKELETON
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-6079 | 48951-6079-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SAFFRON | E849G4X5YJ | ACTIB |
| POTASSIUM ACETATE | M911911U02 | ACTIB |
| SUCROSE | C151H8M554 | IACT |
| ANTIMONY TRISULFIDE | F79059A38U | ACTIB |
| CORALLIUM RUBRUM EXOSKELETON | 2CA71K0DLE | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 0ec36715-4039-6d6f-e063-6394a90af5b6 | c9edf485-e2eb-1605-e053-2a95a90aff2d | 2024-01-12 | Warnings | 0ec36715-4039-6d6f-e063-6394a90af5b6 c9edf485-e2eb-1605-e053-2a95a90aff2d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.