Terra Pure Sanitizing Hand wipe

Manufacturer: Yangzhou Eco-Amenities CO., Ltd
Effective date: 2021-01-19
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:37:05

Label at a glance#

ProductTerra Pure Sanitizing Hand wipe

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Tear open, unfold and apply to hands. For children under 6, use only under adult supervision.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol (alcohol) 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

for external use only: hands

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness occurs.

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

Tear open, unfold and apply to hands.
For children under 6, use only under adult supervision.

Other information

SPL UNCLASSIFIED SECTION

Store between 15-30°C (59-86°F)
Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Didecyldimonium Chloride, Organic Aloe Barbadensis Leaf Juice, Tocopherol, Fragrance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1307051	ethanol 75 % Medicated Pad	PSN	1
1307051	ethanol 0.75 ML/ML Medicated Pad	SCD	1
1307051	ethanol 75 % Hand Sanitizer Wipes	SY	1
1307051	ethyl alcohol 75 % Topical Cloth	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77849-011-00	2022-07-29	C162847	48780-1	e4f33bdf-b123-d8a0-e053-dadaa90a6e4e	Terra Pure Sanitizing Hand wipe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77849-011-00	Terra Pure Sanitizing Hand wipe	3 mL in 1 PATCH	CLOTH	3		1
77849-011-00	Terra Pure Sanitizing Hand wipe	1 in 1 PACKET	CLOTH	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77849-011	TERRA PURE SANITIZING HAND WIPE (ALCOHOL) CLOTH [YANGZHOU ECO-AMENITIES CO., LTD]	1	Legacy NDC, 2 package rows	20210120_b94207f4-9ea6-9b50-e053-2995a90a0c2a.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Terra Pure Sanitizing Hand wipe
ALCOHOL
WATER
DIDECYLDIMONIUM CHLORIDE
ALOE VERA LEAF
TOCOPHEROL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77849-011	77849-011-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
DIDECYLDIMONIUM CHLORIDE	JXN40O9Y9B	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
TOCOPHEROL	R0ZB2556P8	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
b94207f4-9e98-9b50-e053-2995a90a0c2a			b94207f4-9ea6-9b50-e053-2995a90a0c2a	2021-01-19	Warnings	Exact identifier spl id: b94207f4-9e98-9b50-e053-2995a90a0c2a spl set id: b94207f4-9ea6-9b50-e053-2995a90a0c2a

Reported adverse events (FAERS/openFDA)#

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