BainD Ete Alcohol Gel

Manufacturer
Eurocorp Caribbean LLC | Distribuidora cuscatlan
Effective date
2020-09-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:13:38

Label at a glance#

ProductBainD Ete Alcohol Gel
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

AQUA / WATER

ACRYLATES /C 10-30

CROSSPOLYMER

CARBOMER

AMINOMETHYL PROPANOL

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70 %

WARNINGS SECTION

FOR EXTERNAL USE ONLY. FLAMMABLE PRODUCT

KEEP AT A TEMPERATURE NOT HIGHER THAN 105 o F.

MAY DISCOLOR SOME FABRICS, HARMFUL TO WOOD FINISHES.

WHEN USING THIS PRODUCT KEEP OUT OF EYES.

IN CASE OF CONTACT, FLUSH THOROUGHLY WIT WATER.

DO NOT INHALE OR INGEST.

STOP USING AND ASK A DOCTOR : IF IRRITATION AND REDNESS DEVELOP AND PERSISTS FOR MORE THEN 24 HOURS.

DOSAGE FORMS & STRENGTHS SECTION

APPLY A SMALL AMOUNT IN YOUR HANDS AND RUB UNTIL IT DRIES, FOR CHILDREN UNDER 6 USE ONLY UNDER ADULT SUPERVISION.

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.

OTC - PURPOSE SECTION

TO DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASES.

DOSAGE & ADMINISTRATION SECTION

apply a small amount in your hands and rub until it dries, for children under 6. use only under adult supervision.

INDICATIONS & USAGE SECTION

To decrease bateria on the skin that could cause diseases.

PACKAGE LABEL FRONT AND BACK

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABEL FRONT AND BACKLABEL FRONT AND BACK

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75818-400-372022-01-30C16284748780-1d6a99b39-b11f-a426-e053-dadaa90af4c2b016a56d-97a2-632d-e053-2995a90a57dc
75818-400-372022-01-28C16284748780-1d6a99b39-b11f-a426-e053-dadaa90af4c2b016a56d-97a2-632d-e053-2995a90a57dc

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75818-40075818-400-37

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
d6d989a1-7f09-0fc8-e053-2995a90a180db016a56d-97a2-632d-e053-2995a90a57dc2022-01-30WarningsExact identifier
spl set id: b016a56d-97a2-632d-e053-2995a90a57dc

Reported adverse events (FAERS/openFDA)#

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