Cranberry Crush Hand Sanitizer Gel

Manufacturer: Jafra cosmetics International | Jafra Manufacturing, S.A. de C.V.
Effective date: 2020-07-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:21:22

Label at a glance#

ProductCranberry Crush Hand Sanitizer Gel

Active ingredientALCOHOL

Label structure9 sections

Storage and handling

Other information Store at a temperature below 110F (43C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient(s)

Ethyl Alcohol 70% w/v. Purpose: Antimicrobial

OTC - PURPOSE SECTION

Uses

To help reduce bacteria on the skin

INDICATIONS & USAGE SECTION

When using this product keep out of eyes. If contact occurs, rinse thoroughly with water.

WARNINGS SECTION

Warnings

For external use only. Flammable. Keep away from heat or flame

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

Put enough hand sanitizer in your palm to cover hands and rub hands together until dry.
Children under 6 years of age should be supervised when using this product.

STORAGE AND HANDLING SECTION

Other information

Store at a temperature below 110F (43C)
May discolor certain fabrics or surfaces

INACTIVE INGREDIENT SECTION

Inactive ingredients

Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Triethanolamine, Water/Aqua

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Jafra Cranberry Crush

Hand Santizer Gel

Antibacterial

100ml 3.3 fl oz(US)

Tube Cranberry Hand Sanit Gel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68828-246-01	2022-01-28	C162847	48780-1	d6a99b39-ab5d-a426-e053-dadaa90af4c2	Cranberry Crush Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68828-246-01	Cranberry Crush Hand Sanitizer Gel	100 mL in 1 TUBE	GEL	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68828-246	CRANBERRY CRUSH HAND SANITIZER GEL (ALCOHOL) GEL [JAFRA COSMETICS INTERNATIONAL]	1	Legacy NDC, 1 package rows	20200715_aa56f1d4-a3bb-3bf2-e053-2995a90a37c5.zip

Products#

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

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

Cranberry Crush Hand Sanitizer Gel
ALCOHOL
TROLAMINE
GLYCERIN
ALOE VERA LEAF
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68828-246	68828-246-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TROLAMINE	9O3K93S3TK	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	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
aa564d91-4253-4d22-e053-2995a90a3c99			aa56f1d4-a3bb-3bf2-e053-2995a90a37c5	2020-07-13	Warnings	Exact identifier spl id: aa564d91-4253-4d22-e053-2995a90a3c99 spl set id: aa56f1d4-a3bb-3bf2-e053-2995a90a37c5

Reported adverse events (FAERS/openFDA)#

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