PANROSA Instant Hand Sanitizer, Aloe and Moisturizers

Manufacturer: PANROSA ENTERPRISES, INC.
Effective date: 2020-02-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:03:47

Label at a glance#

ProductPANROSA Instant Hand Sanitizer, Aloe and Moisturizers

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin. when water, soap & towel are not available. recommended for repeated use.

Dosage and administration

pump as need into your palms and thoroughly spread on both hands. rub into skin until dry.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

hand sanitizer to help decrease bacteria on the skin. when water, soap & towel are not available.
recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes.

Do not use

OTC - DO NOT USE SECTION

in ears & mouth

When using this product.

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

pump as need into your palms and thoroughly spread on both hands.
rub into skin until dry.

Other information

SPL UNCLASSIFIED SECTION

store at 20°C (68°F to 77°F).
may discolor fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, carbomer, triethanolamine, glycerin, propylene glycol, fragrace, aloe barbadensis leaf juice, FD&C blue No. 1, FD&C yellow No. 5.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

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
50302-002-00	2023-01-30	C162847	48780-1	f386c649-9f09-0266-e053-dadaa90a7c1a	PANROSA Instant Hand Sanitizer, Aloe & Moisturizers

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50302-002-00	PANROSA Instant Hand Sanitizer, Aloe and Moisturizers	237 mL in 1 BOTTLE	GEL	237		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50302-002	PANROSA INSTANT HAND SANITIZER, ALOE AND MOISTURIZERS (ALCOHOL) GEL [PANROSA ENTERPRISES, INC.]	1	Legacy NDC, 1 package rows	20200221_9e3a2f47-3b33-aa30-e053-2a95a90a3379.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

PANROSA Instant Hand Sanitizer, Aloe and Moisturizers
ALCOHOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
GLYCERIN
PROPYLENE GLYCOL
ALOE VERA LEAF
FD&C BLUE NO. 1
FD&C YELLOW NO. 5

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50302-002	50302-002-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
FD&C YELLOW NO. 5	I753WB2F1M	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
9e3a2f47-3b34-aa30-e053-2a95a90a3379			9e3a2f47-3b33-aa30-e053-2a95a90a3379	2020-02-10	Warnings	Exact identifier spl id: 9e3a2f47-3b34-aa30-e053-2a95a90a3379 spl set id: 9e3a2f47-3b33-aa30-e053-2a95a90a3379

Reported adverse events (FAERS/openFDA)#

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