Berry Hand Sanitizer

Manufacturer: K7 Design Group Inc.
Effective date: 2021-06-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:40:40

Label at a glance#

ProductBerry Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 69% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hand-washing to decrease bacteria on the skin, only when water is not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire and flames

For external use only

When using this product

OTC - WHEN USING SECTION

do not get into eyes.
if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop

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 right away

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Carbomer, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Fragrance, Tocopheryl Acetate, Denatonium Benzoate, Red 33, Blue 1.

Product Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Berry

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2287763	ethanol 69 % Topical Gel	PSN	1
2287763	ethanol 0.69 ML/ML Topical Gel	SCD	1
2287763	ethanol 69 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74177-993-01	2023-01-30	C162847	48780-1	f386c64a-02b2-0266-e053-dadaa90a7c1a	Berry Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74177-993-01	Berry Hand Sanitizer	30 mL in 1 BOTTLE, PLASTIC	GEL	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74177-993	BERRY HAND SANITIZER (ALCOHOL) GEL [K7 DESIGN GROUP INC.]	1	Legacy NDC, 1 package rows	20210602_c3b70da1-c2df-edd9-e053-2a95a90a5a2b.zip

Products#

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

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

Berry Hand Sanitizer
Alcohol
ALOE VERA LEAF
AMINOMETHYLPROPANOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
DENATONIUM BENZOATE
GLYCERIN
PROPYLENE GLYCOL
.ALPHA.-TOCOPHEROL ACETATE
D&C RED NO. 33
FD&C BLUE NO. 1

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74177-993	74177-993-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
ALCOHOL	3K9958V90M	ACTIB
DENATONIUM BENZOATE	4YK5Z54AT2	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
FD&C BLUE NO. 1	H3R47K3TBD	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
c3b70da1-c2de-edd9-e053-2a95a90a5a2b			c3b70da1-c2df-edd9-e053-2a95a90a5a2b	2021-06-01	Warnings	Exact identifier spl id: c3b70da1-c2de-edd9-e053-2a95a90a5a2b spl set id: c3b70da1-c2df-edd9-e053-2a95a90a5a2b

Reported adverse events (FAERS/openFDA)#

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