FDA.reportPublic FDA data

Carbo Chamomilla

Manufacturer
Uriel Pharmacy Inc
Effective date
2024-11-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:28:54

Label at a glance#

ProductCarbo Chamomilla
Active ingredientGEUM URBANUM ROOT, BLACK PEPPER, GINGER, ANTIMONY TRISULFIDE, ARSENIC TRIOXIDE, ACORUS CALAMUS ROOT, ACTIVATED CHARCOAL, WORMWOOD, MATRICARIA RECUTITA, GENTIANA LUTEA ROOT
Label structure9 sections

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: Mix 1/4 teaspoon with water. Ages 2-11: Mix 1/8 teaspoon with water. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Carbo betulae (Birch wood charcoal) 2X, Absinthium (Wormwood) 3X, Chamomilla (Chamomile) 3X, Gentiana (Yellow gentian) 3X, Geum urb. (Herb bennet) 3X, Zingiberis (Ginger) 3X, Antimonite (Nat. antimony trisulfide) 4X, Calamus (Sweet flag) 4X, Piper nig. (Black pepper) 5X Arsenicum album (White arsenic) 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Kaolin, Anise oil, Caraway oil, Lactose

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Uses: Temporarily relieves symptoms of upset stomach, diarrhea and flatulence.

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. 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
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carbo Chamomilla PowderCarbo Chamomilla Powder

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3257-4Carbo Chamomilla60 g in 1 BOTTLE, GLASSPOWDER603

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3257CARBO CHAMOMILLA POWDER [URIEL PHARMACY INC]31 package rows20241116_0a5bc3c8-4d62-ccdd-e063-6394a90ab52c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-325748951-3257-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
GEUM URBANUM ROOT33P1Z2B61FACTIB
BLACK PEPPERKM66971LVFACTIB
GINGERC5529G5JPQACTIB
ANTIMONY TRISULFIDEF79059A38UACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
ACORUS CALAMUS ROOTXY1K7KIQ0FACTIB
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
KAOLIN24H4NWX5COIACT
ANISE OIL6Y89129C8HIACT
CARAWAY OILC2J9B08Q3IIACT
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
WORMWOODF84709P2XVACTIB
MATRICARIA RECUTITAG0R4UBI2ZZACTIB
GENTIANA LUTEA ROOTS72O3284MSACTIB

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
26f9dfe3-dd7d-e464-e063-6394a90a11f80a5bc3c8-4d62-ccdd-e063-6394a90ab52c2024-11-15WarningsExact identifier
spl id: 26f9dfe3-dd7d-e464-e063-6394a90a11f8
spl set id: 0a5bc3c8-4d62-ccdd-e063-6394a90ab52c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.