Chimborazo Hand Sanitizer

Manufacturer
Chimborazo LLC
Effective date
2020-12-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:35:24

Label at a glance#

ProductChimborazo Hand Sanitizer
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 10 years of age when using this product to avoid swallowing.

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to the FDA OTC Hand Sanitizer Monograph. The hand sanitizer is manufactured using only the following ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) and Center for Disease Control (CDC) recommendations:

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (70%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerin (1.00% v/v).
  3. Hydrogen peroxide (0.125% v/v).
  4. Sterile water or boiled cold water.
  5. Carbomer 940 (<0.5% v/v)
  6. Tea Tree Oil (0.17% v/v)
  7. Lavender Oil (0.17% v/v)
  8. Triethylamine (<0.2% v/v)
  9. Trace amounts of activated charcoal from filtration of the ethanol

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame. Allergy Alert: Contains Tea Tree Oil.

Do not use

OTC - DO NOT USE SECTION

  • in 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.

Stop use and ask a doctor if irritation or rash occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison

Control Center right away.

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 hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 10 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, water, activated charcoal, carbomer 940, denatonium benzoate, tea tree oil

RECENT MAJOR CHANGES SECTION

Uses

Hand rub to help reduce bacteria on the skin.

Directions

- Place enough product on hands to cover all surfaces. Rub hands until dry.

- Supervise children under 10 years of age when using this product to avoid swallowing.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

General Label:

General LabelGeneral Label

60 mL OR 2 oz. NDC: 80052-001-01:

2 ounce Label2 ounce Label

240 mL OR 8 oz. NDC: 80052-001-02

8 ounce Label8 ounce Label

3785 mL OR 128 oz. NDC: 80052-001-03

128 ounce Label128 ounce Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80052-001-01Chimborazo Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL602
80052-001-02Chimborazo Hand Sanitizer240 mL in 1 BOTTLE, PUMPGEL2402
80052-001-03Chimborazo Hand Sanitizer3786 mL in 1 BOTTLE, PUMPGEL37862

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80052-001CHIMBORAZO HAND SANITIZER (ETHYL ALCOHOL) GEL [CHIMBORAZO LLC]2Legacy NDC, 3 package rows20201217_abfc7e71-2c4c-b4ef-e053-2995a90acce3.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80052-00180052-001-01, 80052-001-02, 80052-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
b6985b0a-3faf-c37b-e053-2a95a90a30c9abfc7e71-2c4c-b4ef-e053-2995a90acce32020-12-16WarningsExact identifier
spl id: b6985b0a-3faf-c37b-e053-2a95a90a30c9
spl set id: abfc7e71-2c4c-b4ef-e053-2995a90acce3