Calm Birch Alcohol Sentinel

Manufacturer
Sunrise Healthcare Technology Limited
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:38

Label at a glance#

ProductCalm Birch Alcohol Sentinel
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Remove the cap and press the top of the head to spray directly on Hand. Body Hair, and household use, then allow approximately 30 seconds for evaporation

Storage and handling

Store under 40˚C (104˚F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% . Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Sanitizes hand, body, hair, and household to reduce bacteria that potentially can cause disease.

Recommended for repeated daily use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

In the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - WHEN USING SECTION

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

if irritation and redness develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Remove the cap and press the top of the head to spray directly on Hand. Body Hair, and household use, then allow approximately 30 seconds for evaporation

Other information

STORAGE AND HANDLING SECTION

Store under 40˚C (104˚F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Parfum, Glycerin, Octoxyglerin, Benzalkonium Chloride, Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelsFront and Back Labels50 mL NDC: 80886-002-01

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
80886-00280886-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
d79d16b5-96b5-361c-e053-2995a90a8a2db29be217-3df0-e7f2-e053-2995a90ac8e72022-02-09WarningsExact identifier
spl set id: b29be217-3df0-e7f2-e053-2995a90ac8e7

Reported adverse events (FAERS/openFDA)#

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