CARE Plus 1 LLC

Manufacturer
Zhejiang Tianbo Daily Necessities Co. Ltd | Care + 1 LLC
Effective date
2021-02-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:21

Label at a glance#

ProductCARE Plus 1 LLC Advanced Hand Sanitizer Wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Open lid, pull back resealable label, remove a wipe for use. Reseal back after use to avoid evaporation of alcohol.

Storage and handling

Dispose of wipe in the proper container. Do not flush down the toilet. Store between 59-86F (15-30C)

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 only 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) (80%, 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. Glycerol (1.45% v/v).
  3. Hydrogen peroxide (0.125% v/v).
  4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

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 and flames

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Open lid, pull back resealable label, remove a wipe for use. Reseal back after use to avoid evaporation of alcohol.

Other information

STORAGE AND HANDLING SECTION

  • Dispose of wipe in the proper container.
  • Do not flush down the toilet.
  • Store between 59-86F (15-30C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), Glycerin, Aloe Barbadensis Leaf Juice (Alose Vera) and Tocopheryl Acetate (Vitamin E)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79901-003-01CARE Plus 1 LLCAdvanced Hand Sanitizer Wipes10 mL in 1 BAGCLOTH101
79901-003-02CARE Plus 1 LLCAdvanced Hand Sanitizer Wipes20 mL in 1 BAGCLOTH201
79901-003-03CARE Plus 1 LLCAdvanced Hand Sanitizer Wipes50 mL in 1 BAGCLOTH501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79901-003CARE PLUS 1 LLC ADVANCED HAND SANITIZER WIPES (ALCOHOL) CLOTH [ZHEJIANG TIANBO DAILY NECESSITIES CO. LTD]1Legacy NDC, 3 package rows20210220_bbb27920-9504-7fff-e053-2a95a90a746a.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79901-00379901-003-01, 79901-003-02, 79901-003-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
bbb27920-9505-7fff-e053-2a95a90a746abbb27920-9504-7fff-e053-2a95a90a746a2021-02-19WarningsExact identifier
spl id: bbb27920-9505-7fff-e053-2a95a90a746a
spl set id: bbb27920-9504-7fff-e053-2a95a90a746a

Reported adverse events (FAERS/openFDA)#

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