Drippn Pure Nature Hand Sanitizer

Manufacturer
iGermx LLC
Effective date
2020-09-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:42

Label at a glance#

ProductDrippn Pure Nature Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 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 Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) 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 0.1854%
  3. Hydrogen peroxide (0.125% v/v).
  4. Water 36.95%
  5. Carbopol 0.824%
  6. Aloe Vera 0.515%
  7. Peppermint 0.215%
  8. AMP 0.1524%
  9. Menthol 0.0515%
  10. Blue 0.00824%

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 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

  • 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. These may be signs of a serious condition.
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 6 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 0.1854%
Hydrogen peroxide (0.125% v/v).
Water 36.95%
Carbopol 0.824%
Aloe Vera 0.515%
Peppermint 0.215%
AMP 0.1524%
Menthol 0.0515%
Blue 0.00824%

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80740-003-04 1 BOTTLE 236 ml

80740-001-0r 1 BOTTLE 8 oz80740-001-0r 1 BOTTLE 8 oz

80740-003-01 1 BOTTLE 1 L

80740-001-01 1 BOTTLE 1 L80740-001-01 1 BOTTLE 1 L

80740-003-02 1 BOTTLE 1 G

80740-001-02 1 BOTTLE 1 G80740-001-02 1 BOTTLE 1 G

80740-003-03 1 BOTTLE 473 ml

80740-001-03 1 BOTTLE 473ml80740-001-03 1 BOTTLE 473ml

80740-003-05 1 BOTTLE 59 ml

80740-001-05 1 BOTTLE 59ml80740-001-05 1 BOTTLE 59ml

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80740-003-01Drippn Pure Nature Hand Sanitizer1000 mL in 1 BOTTLE, PUMPGEL10001
80740-003-02Drippn Pure Nature Hand Sanitizer3785 mL in 1 BOTTLE, PUMPGEL37851
80740-003-03Drippn Pure Nature Hand Sanitizer473 mL in 1 BOTTLE, PUMPGEL4731
80740-003-04Drippn Pure Nature Hand Sanitizer236 mL in 1 BOTTLE, PUMPGEL2361
80740-003-05Drippn Pure Nature Hand Sanitizer59 mL in 1 BOTTLEGEL591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80740-003DRIPPN PURE NATURE HAND SANITIZER (ETHYL ALCOHOL 70%) GEL [IGERMX LLC]1Legacy NDC, 5 package rows20201101_b00c07ea-df43-9cab-e053-2a95a90ac72f.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80740-00380740-003-01, 80740-003-02, 80740-003-03, 80740-003-04, 80740-003-05

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
b00c052b-a53b-6de2-e053-2a95a90a6325b00c07ea-df43-9cab-e053-2a95a90ac72f2020-09-24WarningsExact identifier
spl id: b00c052b-a53b-6de2-e053-2a95a90a6325
spl set id: b00c07ea-df43-9cab-e053-2a95a90ac72f

Reported adverse events (FAERS/openFDA)#

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