Primeauty

Manufacturer: 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 23:07:31

Label at a glance#

ProductPrimeauty Bottle (Pump)

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

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75186-001-01	2022-01-28	C162847	48780-1	d6a99b39-bda2-a426-e053-dadaa90af4c2	Primeauty (PET Bottle w/ pump)
75186-001-02	2022-01-28	C162847	48780-1	d6a99b39-bda2-a426-e053-dadaa90af4c2	Primeauty (PET Bottle w/ pump)
75186-001-03	2022-01-28	C162847	48780-1	d6a99b39-bda2-a426-e053-dadaa90af4c2	Primeauty (PET Bottle w/ pump)
75186-001-04	2022-01-28	C162847	48780-1	d6a99b39-bda2-a426-e053-dadaa90af4c2	Primeauty (PET Bottle w/ pump)
75186-001-05	2022-01-28	C162847	48780-1	d6a99b39-bda2-a426-e053-dadaa90af4c2	Primeauty (PET Bottle w/ pump)
75186-001-06	2022-01-28	C162847	48780-1	d6a99b39-bda2-a426-e053-dadaa90af4c2	Primeauty (PET Bottle w/ pump)
75186-001-07	2022-01-28	C162847	48780-1	d6a99b39-bda2-a426-e053-dadaa90af4c2	Primeauty (PET Bottle w/ pump)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
75186-001-01	PrimeautyBottle (Pump)	240 mL in 1 BOTTLE, PUMP	LIQUID	240	1
75186-001-02	PrimeautyBottle (Pump)	250 mL in 1 BOTTLE, PUMP	LIQUID	250	1
75186-001-03	PrimeautyBottle (Pump)	300 mL in 1 BOTTLE, PUMP	LIQUID	300	1
75186-001-04	PrimeautyBottle (Pump)	350 mL in 1 BOTTLE, PUMP	LIQUID	350	1
75186-001-05	PrimeautyBottle (Pump)	400 mL in 1 BOTTLE, PUMP	LIQUID	400	1
75186-001-06	PrimeautyBottle (Pump)	500 mL in 1 BOTTLE, PUMP	LIQUID	500	1
75186-001-07	PrimeautyBottle (Pump)	1000 mL in 1 BOTTLE, PUMP	LIQUID	1000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75186-001	PRIMEAUTY BOTTLE (PUMP) (ALCOHOL) LIQUID [HUIZHOU DUOMEI DAILY NECESSITIES CO., LTD.]	1	Legacy NDC, 7 package rows	20200423_a3ebb112-80b3-6a54-e053-2995a90a730c.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Primeauty Bottle (Pump)
ALCOHOL
GLYCERIN
WATER
ALOE VERA LEAF
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
ALPHA-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75186-001	75186-001-01, 75186-001-02, 75186-001-03, 75186-001-04, 75186-001-05, 75186-001-06, 75186-001-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a3ebb123-c493-13fe-e053-2a95a90a0842			a3ebb112-80b3-6a54-e053-2995a90a730c	2020-04-22	Warnings	Exact identifier spl id: a3ebb123-c493-13fe-e053-2a95a90a0842 spl set id: a3ebb112-80b3-6a54-e053-2995a90a730c

Reported adverse events (FAERS/openFDA)#

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