FDA.reportPublic FDA data

Carbo Chamomilla

Manufacturer
Uriel Pharmacy Inc.
Effective date
2026-08-14
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-08-18 02:01:49

Label at a glance#

ProductCarbo Chamomilla
Active ingredientANTIMONY TRISULFIDE, MATRICARIA RECUTITA, WORMWOOD, GENTIANA LUTEA ROOT, ARSENIC TRIOXIDE, ACORUS CALAMUS ROOT, GEUM URBANUM ROOT, GINGER, BLACK PEPPER
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Ages 12 and older: 1 capsule 3-4 times daily.
Under age 11: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Antimonite (Nat. antimony trisulfide) 3X, Chamomilla e rad. (Chamomile) 3X, Geum urbanum e rad. (Herb bennet) 3X, Absinthium ex herba (Wormwood) 5X, Gentiana e rad. (Yellow gentian) 5X, Zingiberis e rhiz. (Ginger) 5X, Arsenicum album (White arsenic) 6X, Calamus e rhiz. (Sweet flag) 6X, Piper nig. e fruct. (Black pepper) 7X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Carbo Fagi, Vegetable capsules, 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 CapsulesCarbo Chamomilla Capsules

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-3216-72026-01-29C16284748780-149896155-a0e3-586f-e063-e6dba90add90Carbo Chamomilla
48951-3216-72026-01-29C16284748780-149896155-a0e3-586f-e063-e6dba90add90Carbo Chamomilla

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
48951-321648951-3216-7

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
ANTIMONY TRISULFIDEF79059A38UACTIB
MATRICARIA RECUTITAG0R4UBI2ZZACTIB
WORMWOODF84709P2XVACTIB
GENTIANA LUTEA ROOTS72O3284MSACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
ACORUS CALAMUS ROOTXY1K7KIQ0FACTIB
GEUM URBANUM ROOT33P1Z2B61FACTIB
GINGERC5529G5JPQACTIB
BLACK PEPPERKM66971LVFACTIB
ACTIVATED CHARCOAL2P3VWU3H10IACT
POWDERED CELLULOSESMD1X3XO9MIACT
ANISE OIL6Y89129C8HIACT
CARAWAY OILC2J9B08Q3IIACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-11-15full-release2026-06-01 02:28:56

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
Carbo ChamomillaCARBO CHAMOMILLAUriel Pharmacy Inc.6bc88bd3-ffe9-46d7-e053-2a91aa0acf792026-08-14WarningsExact identifier
ndc (package): 48951-3216-7
ndc (product): 48951-3216
ndc11 (package): 48951321607
spl id: 5907ec1f-624e-81d5-e063-6394a90a2b91
spl set id: 6bc88bd3-ffe9-46d7-e053-2a91aa0acf79

Reported adverse events (FAERS/openFDA)#

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