MyTerra Hand Sanitizer Foam

Manufacturer
PortionPac Chemical Corporation
Effective date
2020-03-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:37:58

Label at a glance#

ProductMyTerra Hand Sanitizer Foam
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Pump a small amount of foam into palm of hand. Spread on hands and rub into skin until dry. Pump a smaller amount into one hand and spread over both hands and wrists. Rub into skin until dry. Children should be supervised while using this product.

Label contents#

Full prescribing information#

​Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% v/v

​Purpose

OTC - PURPOSE SECTION

Skin Sanitizer

​Use

INDICATIONS & USAGE SECTION

To help reduce the amount of bacteria on skin

​Warnings

WARNINGS SECTION

Flammable.  Keep away from fire or flame.

For external use only.  If swallowed seek medical attention.

When using this product do not use around or near the eyes.  If contact occurs, flush eyes with water and contact a doctor immediately.

Stop use and consult a doctor when skin irritation appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

​Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount of foam into palm of hand.
  • Spread on hands and rub into skin until dry.
  • Pump a smaller amount into one hand and spread over both hands and wrists.
  • Rub into skin until dry.
  • Children should be supervised while using this product.

​Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycerin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Case Label - 8 x 1000 mLCase Label - 8 x 1000 mL

Products#

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DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70780-15270780-152-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
b70309dc-fb78-4da1-a4bf-65240d11bb0b558a1b59-2d14-4847-aecd-a56301e08c092020-03-20WarningsExact identifier
spl id: b70309dc-fb78-4da1-a4bf-65240d11bb0b
spl set id: 558a1b59-2d14-4847-aecd-a56301e08c09

Reported adverse events (FAERS/openFDA)#

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