Primeauty

Manufacturer
Huizhou New Road Cosmetics Company Limited | Huizhou Duomei Daily Necessities Co., Ltd.
Effective date
2020-04-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:32

Label at a glance#

ProductPrimeauty Squeeze Tube
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

For hand washing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Put enough product on hands to cover all surfaces. Rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 110F (43C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

  • Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
  • for external use only.
  • Flammable, keep away from heat and flame

OTC - STOP USE SECTION

  • Stop use and ask a doctor if
  • irritation and redness develop and persist for more than 72 hours
  • Swallowed, get medical help or contact a poison control center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put enough product on hands to cover all surfaces. Rub hands together until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store below 110F (43C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Triethanolamine, Tocopheryl Acetate, Aloe

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75150-002-01PrimeautySqueeze Tube10 mL in 1 TUBELIQUID101
75150-002-02PrimeautySqueeze Tube20 mL in 1 TUBELIQUID201
75150-002-03PrimeautySqueeze Tube30 mL in 1 TUBELIQUID301
75150-002-04PrimeautySqueeze Tube50 mL in 1 TUBELIQUID501
75150-002-05PrimeautySqueeze Tube60 mL in 1 TUBELIQUID601
75150-002-06PrimeautySqueeze Tube80 mL in 1 TUBELIQUID801
75150-002-07PrimeautySqueeze Tube100 mL in 1 TUBELIQUID1001
75150-002-08PrimeautySqueeze Tube150 mL in 1 TUBELIQUID1501
75150-002-09PrimeautySqueeze Tube200 mL in 1 TUBELIQUID2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75150-002PRIMEAUTY SQUEEZE TUBE (ETHYL ALCOHOL) LIQUID [HUIZHOU NEW ROAD COSMETICS COMPANY LIMITED]1Legacy NDC, 9 package rows20200423_a3edc10e-761c-c49e-e053-2995a90aa84d.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
a3ecf9f6-4011-74c3-e053-2a95a90a7766a3edc10e-761c-c49e-e053-2995a90aa84d2020-04-22WarningsExact identifier
spl id: a3ecf9f6-4011-74c3-e053-2a95a90a7766
spl set id: a3edc10e-761c-c49e-e053-2995a90aa84d

Reported adverse events (FAERS/openFDA)#

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