Terra Pure Spa Collection Fresh Aloe Hand Sanitizer

Manufacturer
Yangzhou Eco-Amenities CO., Ltd
Effective date
2020-08-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:49

Label at a glance#

ProductTerra Pure Spa Collection Fresh Aloe Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. For children under 6, use only under adult supervision.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 69.99% v/v

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 or 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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • 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 (140°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Dichlorobenzyl alcohol, Acrylates/C10-30 alkyl acrylate crosspolymer, Triethanolamine, Methyl Gluceth-20, Glycerin, Organic Aloe Barbadensis Leaf Juice, Tocopherol, Fragrance

Package Labeling:77849-007-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Package Labeling:77849-007-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Package Labeling:77849-007-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5Label5

Package Labeling:77849-007-03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label7Label7

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2370157ethanol 69.9 % Topical GelPSN1
2370157ethanol 0.699 ML/ML Topical GelSCD1
2370157ethanol 69.9 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77849-007-00Terra Pure Spa Collection Fresh Aloe Hand Sanitizer30 mL in 1 BOTTLEGEL301
77849-007-01Terra Pure Spa Collection Fresh Aloe Hand Sanitizer50 mL in 1 BOTTLEGEL501
77849-007-02Terra Pure Spa Collection Fresh Aloe Hand Sanitizer500 mL in 1 BOTTLEGEL5001
77849-007-03Terra Pure Spa Collection Fresh Aloe Hand Sanitizer3800 mL in 1 BOTTLEGEL38001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77849-007TERRA PURE SPA COLLECTION FRESH ALOE HAND SANITIZER (ALCOHOL) GEL [YANGZHOU ECO-AMENITIES CO., LTD]1Legacy NDC, 4 package rows20200815_acdba1fa-1082-62df-e053-2995a90a7570.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77849-00777849-007-00, 77849-007-01, 77849-007-02, 77849-007-03

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
acdba1fa-1083-62df-e053-2995a90a7570acdba1fa-1082-62df-e053-2995a90a75702020-08-14WarningsExact identifier
spl id: acdba1fa-1083-62df-e053-2995a90a7570
spl set id: acdba1fa-1082-62df-e053-2995a90a7570

Reported adverse events (FAERS/openFDA)#

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