FDA.reportPublic FDA data

LACTOSE, UNSPECIFIED FORM

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-12-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:29:24

Label at a glance#

ProductCinis comp.
Active ingredientTOBACCO LEAF, EQUISETUM ARVENSE TOP, QUERCUS ROBUR WHOLE
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: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Cinis Equiseti (Ash of horsetail herb) 6X, Cinis Quercus (Decoction of oak bark ash) 6X, Cinis Tabaci (Tobacco ash) 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 20% Organic cane alcohol, Lactose

Prepared using rhythmical processes.

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. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. Contains traces of lactose. 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

Cinis comp. LiquidCinis comp. Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3242-3Cinis comp.60 mL in 1 BOTTLE, DROPPERLIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3242CINIS COMP. LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20241208_bcb9d2bc-1492-6aff-e053-2995a90a1e44.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-324248951-3242-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
WATER059QF0KO0RIACT
TOBACCO LEAF6YR2608RSUACTIB
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
QUERCUS ROBUR WHOLER7QMG0BT2WACTIB
ALCOHOL3K9958V90MIACT

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
289f2edc-5ed6-f34a-e063-6294a90a3f4cbcb9d2bc-1492-6aff-e053-2995a90a1e442024-12-06WarningsExact identifier
spl id: 289f2edc-5ed6-f34a-e063-6294a90a3f4c
spl set id: bcb9d2bc-1492-6aff-e053-2995a90a1e44

Reported adverse events (FAERS/openFDA)#

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