Ultra Defense Sani Smart Hand Sanitizing Wipes

Manufacturer: K7 Design Group Inc.
Effective date: 2020-08-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:25:58

Label at a glance#

ProductUltra Defense Sani Smart Hand Sanitizing Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Indications and uses

For hand sanitizing to decrease bactera on the skin. Apply topically to the skin to help prevent cross contamination. Recommended for repeated use. Dries in seconds.

Dosage and administration

Remove lid and discard seal from container. Pull wipe from center of roll and thread through opening in lid. Do not push finger through opening. Replace lid, pull wipe up, and then out at a 45º angle. The next wipe dispenses automatically. Close lid to retain moisture.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bactera on the skin.
Apply topically to the skin to help prevent cross contamination.
Recommended for repeated use.
Dries in seconds.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

do not use in or contact the eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

too much skin irritation or sensitivity develops or increases.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Remove lid and discard seal from container.
Pull wipe from center of roll and thread through opening in lid.
Do not push finger through opening.
Replace lid, pull wipe up, and then out at a 45º angle. The next wipe dispenses automatically.
Close lid to retain moisture.

Other information

OTHER SAFETY INFORMATION

Lot No. Manufacture date and Expiration date can be found on canister.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Ethyl Alcohol, DMDM Hydantoin, Glycerin, Propylene Glycol, Cocamidopropyl Betaine, Decyl glucoside, Aloe Barbadensis Leaf Extract

Product Packaging - 70 COUNT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ULTRA DEFENSE

SANI+SMART

HAND

SANITIZING

WIPES

70 COUNT

COTTON SOFT WIPES

KILLS 99.99% OF GERMS

5.71 in x 8.07 in (14.5cm x 20.5cm)

wipes

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1038558	benzalkonium chloride 0.13 % Medicated Pad	PSN	1
1038558	benzalkonium chloride 1.3 MG/ML Medicated Pad	SCD	1
1038558	benzalkonium chloride 0.13 % Topical Cloth	SY	1
1038558	benzalkonium chloride 0.13 % Topical Swab	SY	1
1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Pad	SY	1
1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Swab	SY	1
1038558	benzalkonium chloride 1 ML per 750 ML Topical Swab	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74177-850-70	2022-01-28	C162847	48780-1	d6a99b39-c854-a426-e053-dadaa90af4c2	Ultra Defense Sani Smart Hand Sanitizing Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74177-850-70	Ultra Defense Sani Smart Hand Sanitizing Wipes	191 g in 1 CANISTER	CLOTH	191		1
74177-850-70	Ultra Defense Sani Smart Hand Sanitizing Wipes	70 in 1 CANISTER	CLOTH	70		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74177-850	ULTRA DEFENSE SANI SMART HAND SANITIZING WIPES (BENZALKONIUM CHLORIDE) CLOTH [K7 DESIGN GROUP INC.]	1	Legacy NDC, 2 package rows	20200827_adcbaa6d-0f76-1a12-e053-2a95a90ac8d8.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Ultra Defense Sani Smart Hand Sanitizing Wipes
Benzalkonium Chloride
BENZALKONIUM
COCAMIDOPROPYL BETAINE
DMDM HYDANTOIN
DECYL GLUCOSIDE
ALOE VERA LEAF
WATER
PHENOXYETHANOL
ALCOHOL
GLYCERIN
PROPYLENE GLYCOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74177-850	74177-850-70

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
DECYL GLUCOSIDE	Z17H97EA6Y	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
ALCOHOL	3K9958V90M	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT

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
adcbaed0-6127-ba94-e053-2995a90a3e6d			adcbaa6d-0f76-1a12-e053-2a95a90ac8d8	2020-08-26	Warnings	Exact identifier spl id: adcbaed0-6127-ba94-e053-2995a90a3e6d spl set id: adcbaa6d-0f76-1a12-e053-2a95a90ac8d8

Reported adverse events (FAERS/openFDA)#

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