Bama Bio Tech Hand Sanitizer 70 Ethanol LemonGrass Scent

Manufacturer
Bama-Bio Tech Corporation
Effective date
2021-08-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:42:37

Label at a glance#

ProductBama Bio Tech Hand Sanitizer 70 Ethanol LemonGrass Scent
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

PLACE PRODUCT ON HANDS TO COVER ALL SURFACES. RUB HANDS TOGETHER UNTIL DRY. SUPERVISE USE CHILDREN UNDER 6 YEARS OF AGE.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT[S]

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 70% v/v

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USE[S]

INDICATIONS & USAGE SECTION

HEALTHCARE PERSONNEL HAND RUB TO HELP REDUCE BACTERIA THAT POTENTIALLY CAN CAUSE DISEASE.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY. FLAMMABLE. KEEP AWAY FROM HEAT OR FLAME. 

DO NOT USE

OTC - DO NOT USE SECTION

  • ON CHILDREN UNDER 2 MONTHS OF AGE
  • ON OPEN SKIN WOUNDS

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

KEEP OUT OF EYES, EARS, AND MOUTH. IN CASE OF CONTACT WITH EYES, RINSE EYES THOROUGHLY WITH WATER.

STOP USE AND CONTACT A PHYSICIAN

OTC - STOP USE SECTION

IF IRRITATION OR RASH OCCUR.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IF SWALLOWED, CALL POISON CONTROL IMMEDIATELY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

PLACE PRODUCT ON HANDS TO COVER ALL SURFACES. RUB HANDS TOGETHER UNTIL DRY. SUPERVISE USE CHILDREN UNDER 6 YEARS OF AGE.

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

STORE BETWEEN 15-30°C (59-86°F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

PURIFIED WATER USP, GLYCERIN, LAURYL LACTATE, HYDROXYPROPYLCELLULOSE (HPC), ALOE VERA GEL, HYDROGEN PEROXIDE, NATURAL ESSENTIAL OILS.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label9Label9

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
90085-002-012023-01-30C16284748780-1f386c64a-09e5-0266-e053-dadaa90a7c1aBama-Bio Tech Hand Sanitizer 70% Ethanol LemonGrass Scent

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90085-002-01Bama Bio Tech Hand Sanitizer 70 Ethanol LemonGrass Scent946 mL in 1 BOTTLEGEL9463

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90085-002BAMA BIO TECH HAND SANITIZER 70 ETHANOL LEMONGRASS SCENT (ALCOHOL) GEL [BAMA-BIO TECH CORPORATION]3Legacy NDC, 1 package rows20211007_227f9df8-0f1a-4ae2-a8bb-d260a3e41086.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90085-00290085-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
ca014d7b-6d6e-3245-e053-2995a90a990e227f9df8-0f1a-4ae2-a8bb-d260a3e410862021-08-20WarningsExact identifier
spl id: ca014d7b-6d6e-3245-e053-2995a90a990e
spl set id: 227f9df8-0f1a-4ae2-a8bb-d260a3e41086

Reported adverse events (FAERS/openFDA)#

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