BLOW ME by Assholes live forever

Manufacturer
Guangzhou Oumiao Cosmetics Co. Ltd.
Effective date
2020-10-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:31:16

Label at a glance#

ProductBLOW ME
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

external usage products, spray on neck , wrist and other surfaces of skin .

Dosage and administration

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 106°F.(40℃)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL80%

Purpose

OTC - PURPOSE SECTION

Solven

Uses

INDICATIONS & USAGE SECTION

external usage products, spray on neck , wrist and other surfaces of skin .

Warnings

WARNINGS SECTION

1.Caution for those who are allergic to ethanol (alcohol).
2.Should be stored in a cool and dry place, away from fire.
3.For external use only.

When using this product, do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - DO NOT USE SECTION

do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.

When using this product

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.

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

Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store below 106°F.(40℃)

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, PARFUM

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74761-012-01 50ml74761-012-01 50ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN2
1039339ethanol 0.8 ML/ML Topical SolutionSCD2
1039339ethanol 80 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74761-016-012022-01-28C16284748780-1d6a99b39-62e0-a426-e053-dadaa90af4c274761-016 BLOW ME

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74761-016-01BLOW ME50 mL in 1 BOTTLELIQUID502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74761-016BLOW ME LIQUID [GUANGZHOU OUMIAO COSMETICS CO. LTD. ]2Legacy NDC, 1 package rows20201009_af5685aa-0973-277c-e053-2a95a90ace1b.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74761-01674761-016-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
DISPERSE RED 1515FG1M8OP9IACT
WATER059QF0KO0RIACT

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
b12545eb-4f05-7d40-e053-2995a90a26adaf5685aa-0973-277c-e053-2a95a90ace1b2020-10-08WarningsExact identifier
spl id: b12545eb-4f05-7d40-e053-2995a90a26ad
spl set id: af5685aa-0973-277c-e053-2a95a90ace1b

Reported adverse events (FAERS/openFDA)#

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