FDA.reportPublic FDA data

Green Goo Hand Sanitizer

Manufacturer
Sierra Sage Herbs, LLC
Effective date
2020-11-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:09

Label at a glance#

ProductGreen Goo Hand Sanitizer
Active ingredientALCOHOL
Label structure15 sections

Indications and uses

Hand sanitizer to help reduce microbes that potentially can cause disease For use when soap and water are not available

Dosage and administration

Place enough product on hand to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

70% v/v Ethyl Alcohol

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce microbes that potentially can cause disease

  • For use when soap and water are not available

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hand to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Carbomer, Natural Lavender, Aminomethyl Propanol.

Questions or comments?

OTC - QUESTIONS SECTION

1-888-613-4972

SPL UNCLASSIFIED SECTION

Sierra Sage® Herbs LLC 424 Main Streen Lyons, CO 80540 USA

Principal Display Panel 3oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GREEN GOO®

THIS TUBE IS MADE

FROM SUGARCANE

100% RECYCLABLE

ISO CERTIFIED

FDA APPROVED

BPA FREE

HAND SANITIZER

LAVENDER

A spicy, sweet, floral aroma

3.0 FL. OZ (88.5 ML.)

Natural_Lavender_3.jpgNatural_Lavender_3.jpg

Principal Display Panel 1oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GREEN GOO®

THIS TUBE IS MADE

FROM SUGARCANE

100% RECYCLABLE

ISO CERTIFIED

FDA APPROVED

BPA FREE

HAND SANITIZER

LAVENDER

A spicy, sweet, floral aroma

1.0 FL. OZ (29.5 ML.)

Natural_Lavender_1.jpgNatural_Lavender_1.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70994-336-012025-01-30C16284748780-12cef2736-7efc-d83d-e063-dadaa90ab31fGreen Goo - Natural Lavender
70994-336-022025-01-30C16284748780-12cef2736-7efc-d83d-e063-dadaa90ab31fGreen Goo - Natural Lavender

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70994-336-01Green Goo Hand Sanitizer88.5 mL in 1 TUBEGEL88.51
70994-336-02Green Goo Hand Sanitizer29.5 mL in 1 TUBEGEL29.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70994-336GREEN GOO HAND SANITIZER (ETHYL ALCOHOL 70%) GEL [SIERRA SAGE HERBS, LLC]1Legacy NDC, 2 package rows20201124_b479725f-720f-bc02-e053-2a95a90aadea.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70994-33670994-336-01, 70994-336-02

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
NameUNIIKind
LAVENDER OILZBP1YXW0H8IACT
ALCOHOL3K9958V90MACTIB
ISOPROPYL ALCOHOLND2M416302IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER 9804Q93RCW27EIACT
WATER059QF0KO0RIACT

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
b479725f-7210-bc02-e053-2a95a90aadeab479725f-720f-bc02-e053-2a95a90aadea2020-11-19WarningsExact identifier
spl id: b479725f-7210-bc02-e053-2a95a90aadea
spl set id: b479725f-720f-bc02-e053-2a95a90aadea

Reported adverse events (FAERS/openFDA)#

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