70% Pana Instant Hand Sanitizer

Manufacturer: PL COSMETIC
Effective date: 2020-04-28
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:08:23

Label at a glance#

Product70% Pana Instant Hand Sanitizer

Active ingredientALCOHOL

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70 PERCENT PANA

WARNINGS SECTION

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - DO NOT USE SECTION

OTC - PURPOSE SECTION

OTC - STOP USE SECTION

INDICATIONS & USAGE SECTION

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
74339-7570-1	2024-01-30	C162847	48780-1	1030e364-fde4-111a-e063-dadaa90a10e2	70% Pana Instant Hand Sanitizer 74339-7570-1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74339-7570-1	70% Pana Instant Hand Sanitizer	500 mL in 1 BOTTLE, PUMP	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74339-7570	70% PANA INSTANT HAND SANITIZER (ALCOHOL) GEL [PL COSMETIC]	1	Legacy NDC, 1 package rows	20200428_a455a738-675f-b160-e053-2a95a90a68d2.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

70% Pana Instant Hand Sanitizer
ALCOHOL
PANTHENOL
MENTHA ARVENSIS LEAF OIL
GLYCERIN
.ALPHA.-TOCOPHEROL ACETATE
ALOE VERA LEAF
WATER
AMINOMETHYL PROPANEDIOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
HYALURONATE SODIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74339-7570	74339-7570-1

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
PANTHENOL	WV9CM0O67Z	IACT
MENTHA ARVENSIS LEAF OIL	1AEY1M553N	IACT
GLYCERIN	PDC6A3C0OX	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
AMINOMETHYL PROPANEDIOL	CZ7BU4QZJZ	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
HYALURONATE SODIUM	YSE9PPT4TH	IACT
ALCOHOL	3K9958V90M	ACTIB

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
a455d835-c887-10d3-e053-2a95a90a94c6			a455a738-675f-b160-e053-2a95a90a68d2	2020-04-28		Exact identifier spl id: a455d835-c887-10d3-e053-2a95a90a94c6 spl set id: a455a738-675f-b160-e053-2a95a90a68d2

Reported adverse events (FAERS/openFDA)#

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