KENDA CARE INSTANT HAND SANITIZER

Manufacturer: MICRO CONNECTION ENTERPRISES INC
Effective date: 2023-03-01
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:54:20

Label at a glance#

ProductKENDA CARE INSTANT HAND SANITIZER 70 PERCENT

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

Dispense directly on hands and rub in thoroughly. Children under 6 should be helped and supervised.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70% W/V

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

USE

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin that could cause disease.

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat and flame. Do not inhale or ingest. Keep out of eyes, ears, and mouth. If eye contact occurs, flush thoroughly with water and seek medical advice. Avoid contact with broken skin. Not for use on infants. Stop use and ask a doctor if irritation, rash, or redness occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Dispense directly on hands and rub in thoroughly.
Children under 6 should be helped and supervised.

OTHER INFORMATION

OTHER SAFETY INFORMATION

Store between 15°C and 37°C (59°F and 99°F). Avoid freezing. Avoid excessive heat above 40°C (104°F).

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Glycerin, Aminomethyl Propanol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Kenda Care_Hand Sani Gel_10oz

01b LBL_Kenda Care_Hand Sani Gel_16.9oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	3
581662	ethanol 0.7 ML/ML Topical Gel	SCD	3
581662	ethanol 70 % Topical Gel	SY	3
581662	ethyl alcohol 70 % Topical Gel	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76038-404-10	2025-01-30	C162847	48780-1	f386c649-edd2-0266-e053-dadaa90a7c1a	PCPG (as CMO) - KENDA CARE INSTANT HAND SANITIZER - 70% ETHYL ALCOHOL (76038-404)
76038-404-17	2025-01-30	C162847	48780-1	f386c649-edd2-0266-e053-dadaa90a7c1a	PCPG (as CMO) - KENDA CARE INSTANT HAND SANITIZER - 70% ETHYL ALCOHOL (76038-404)
76038-404-10	2023-03-01	C162847	48780-1	f386c649-edd2-0266-e053-dadaa90a7c1a	PCPG (as CMO) - KENDA CARE INSTANT HAND SANITIZER - 70% ETHYL ALCOHOL (76038-404)
76038-404-17	2023-03-01	C162847	48780-1	f386c649-edd2-0266-e053-dadaa90a7c1a	PCPG (as CMO) - KENDA CARE INSTANT HAND SANITIZER - 70% ETHYL ALCOHOL (76038-404)
76038-404-10	2023-01-30	C162847	48780-1	f386c649-edd2-0266-e053-dadaa90a7c1a	PCPG (as CMO) - KENDA CARE INSTANT HAND SANITIZER - 70% ETHYL ALCOHOL (76038-404)
76038-404-17	2023-01-30	C162847	48780-1	f386c649-edd2-0266-e053-dadaa90a7c1a	PCPG (as CMO) - KENDA CARE INSTANT HAND SANITIZER - 70% ETHYL ALCOHOL (76038-404)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76038-404-10	KENDA CARE INSTANT HAND SANITIZER70 PERCENT	300 mL in 1 BOTTLE	GEL	300		3
76038-404-17	KENDA CARE INSTANT HAND SANITIZER70 PERCENT	500 mL in 1 BOTTLE	GEL	500		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76038-404	KENDA CARE INSTANT HAND SANITIZER 70 PERCENT (ETHYL ALCOHOL) GEL [MICRO CONNECTION ENTERPRISES INC]	3	Legacy NDC, 2 package rows	20230302_bd8071e3-0596-4ed5-a9f4-e607209547d5.zip

Products#

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

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

KENDA CARE INSTANT HAND SANITIZER 70 PERCENT
ETHYL ALCOHOL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
AMINOMETHYLPROPANOL
GLYCERIN
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76038-404	76038-404-17, 76038-404-10

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f5dc9661-fa30-f1e1-e053-2995a90ab892			bd8071e3-0596-4ed5-a9f4-e607209547d5	2023-03-01	Warnings	Exact identifier spl id: f5dc9661-fa30-f1e1-e053-2995a90ab892 spl set id: bd8071e3-0596-4ed5-a9f4-e607209547d5

Reported adverse events (FAERS/openFDA)#

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