Hand Antibacterial

Manufacturer: Herstyler, Inc.
Effective date: 2020-05-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:13:36

Label at a glance#

ProductHand Antibacterial Alcohol Free with Lavender

Active ingredientBENZALKONIUM CHLORIDE

Label structure10 sections

Indications and uses

■ For Handwashing to help reduce bacteria on the skin.

Dosage and administration

■ Wet hands. Apply a palmful to hands. ■ Scrub thoroughly for at least 30 seconds and then rinse. ■ Supervise children under 6 years of age when using this product to avoid swallowing

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ For Handwashing to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

■ keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes throughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develops and persists.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, contact a doctor or Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Wet hands. Apply a palmful to hands. ■ Scrub thoroughly for at least 30 seconds and then rinse. ■ Supervise children under 6 years of age when using this product to avoid swallowing

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Glyceryl Laurate, Phenoxyethanol, Fragrance, PEG-150 Distearate, Lavender (Lavandula Angustifolia) Flower Oil, Disodium EDTA, Citric Acid, Magnesium Chloride, Methylchloroisothiazoline, Magnesium Nitrate, Methylisothiazolinone

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	1
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	1
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	1
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75177-020-16	2022-01-28	C162847	48780-1	d6a99b39-c07b-a426-e053-dadaa90af4c2	Beautyfrizz Hand Sanitizer bzk Lavender

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75177-020-16	Hand AntibacterialAlcohol Free with Lavender	500 mL in 1 BOTTLE, PUMP	LIQUID	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75177-020	HAND ANTIBACTERIAL ALCOHOL FREE WITH LAVENDER (BENZALKONIUM CHLORIDE) LIQUID [HERSTYLER, INC.]	1	Legacy NDC, 1 package rows	20200519_a5ef3ae7-484e-9eba-e053-2995a90a0cbb.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

Hand Antibacterial Alcohol Free with Lavender
Benzalkonium chloride
MAGNESIUM CHLORIDE
METHYLISOTHIAZOLINONE
GLYCERYL LAURATE
PHENOXYETHANOL
COCAMIDOPROPYL BETAINE
SODIUM LAURETH SULFATE
LAVENDER OIL
PEG-150 DISTEARATE
WATER
BENZALKONIUM
SODIUM CHLORIDE
MAGNESIUM NITRATE
EDETATE SODIUM
METHYLCHLOROISOTHIAZOLINONE
ANHYDROUS CITRIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75177-020	75177-020-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MAGNESIUM CHLORIDE	02F3473H9O	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
GLYCERYL LAURATE	Y98611C087	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
SODIUM LAURETH SULFATE	BPV390UAP0	IACT
LAVENDER OIL	ZBP1YXW0H8	IACT
PEG-150 DISTEARATE	6F36Q0I0AC	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
SODIUM CHLORIDE	451W47IQ8X	IACT
MAGNESIUM NITRATE	77CBG3UN78	IACT
EDETATE SODIUM	MP1J8420LU	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT

Source Document#

Source XML · Source PDF

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
a5ef3667-66f1-7e89-e053-2995a90a94ae			a5ef3ae7-484e-9eba-e053-2995a90a0cbb	2020-05-18	Warnings	Exact identifier spl id: a5ef3667-66f1-7e89-e053-2995a90a94ae spl set id: a5ef3ae7-484e-9eba-e053-2995a90a0cbb

Reported adverse events (FAERS/openFDA)#

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