Hand Sanitizer

Manufacturer
Beyond Health P.A. | Derma Care Research Labs, LLC
Effective date
2023-01-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:41:23

Label at a glance#

ProductHand Sanitizer Dr. Butler
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

OTC - PURPOSE SECTION


Antiseptic

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

WARNINGS SECTION

For external use only. Flammable-keep away from fire or flame. When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water, avoid contact with broken skin, and do not inhale or ingest. Stop use and ask a doctor if rash or irritation develops and lasts for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Tocopheryl Acetate, Glycerin, Propylene Glycol, Isopropyl Myristate, Carbomer, Aminomethyl Propanol.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70942-157-082025-01-30C16284748780-12cef2736-a8b2-d83d-e063-dadaa90ab31fHand Sanitizer

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70942-157HAND SANITIZER DR. BUTLER (ETHYL ALCOHOL) GEL [BEYOND HEALTH P.A.]2Legacy NDC20230110_a1c48934-6e9d-dba6-e053-2995a90ab05d.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70942-15770942-157-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
f1d91cd2-6d14-3e7b-e053-2a95a90ab05ca1c48934-6e9d-dba6-e053-2995a90ab05d2023-01-09WarningsExact identifier
spl id: f1d91cd2-6d14-3e7b-e053-2a95a90ab05c
spl set id: a1c48934-6e9d-dba6-e053-2995a90ab05d

Reported adverse events (FAERS/openFDA)#

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