CAREONE

Manufacturer
American Sales Company | Apollo Health and Beauty Care Inc.
Effective date
2017-04-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:40

Label at a glance#

ProductCAREONE Instant Hand Sanitizer with Moisturizers and Vitamin E
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

to help reduce bacteria on the skin.

Dosage and administration

put enough product in your palm to cover hands and rub hands together until dry. children under 6 years should be supervised when using this product.

Storage and handling

store at a temperature below 110°F (43°C) may discolor some fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from source of heat or fire.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develops and lasts.
Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • put enough product in your palm to cover hands and rub hands together until dry.
  • children under 6 years should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • store at a temperature below 110°F (43°C)
  • may discolor some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Carbomer, Aminomethyl Propanol, Fragrance (Parfum).

Label Copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of the labelImage of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN1
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD1
808520isopropyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41520-178-162020-01-31C16284748780-19d75b9cf-fee7-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41520-178-16CAREONEInstant Hand Sanitizer with Moisturizers and Vitamin E443 mL in 1 BOTTLE, PLASTICLIQUID4431

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41520-178CAREONE INSTANT HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E (ETHYL ALCOHOL) LIQUID [AMERICAN SALES COMPANY]1Legacy NDC, 1 package rows20170427_f722f9e2-74e5-48b7-a7e4-9f7e79438b50.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
41520-17841520-178-16

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
833eefb3-aad7-43c5-a51d-c611f9f697f3f722f9e2-74e5-48b7-a7e4-9f7e79438b502017-04-26WarningsExact identifier
spl id: 833eefb3-aad7-43c5-a51d-c611f9f697f3
spl set id: f722f9e2-74e5-48b7-a7e4-9f7e79438b50

Reported adverse events (FAERS/openFDA)#

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