FDA.reportPublic FDA data

BQ Pharma Hand Sanitizer

Manufacturer
Frank por Laboratories, S.A. de C.V.
Effective date
2020-08-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:31:13

Label at a glance#

ProductBQ Pharma Hand Sanitizer
Active ingredientALCOHOL
Label structure19 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from jeat or flame.

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • On open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears and mouth. I case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

SPL UNCLASSIFIED SECTION

  • Do not store above 105ºF (40ºC)
  • May discolor certain wood surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Camphor, Carbomer, Glycerin, Menthol, Triethanolamine, Water.

Questions or comments?

OTC - QUESTIONS SECTION

#-###-###-###

*Mix of mostiurizers that will keep your hands moisturized for up to 24 hours.

Made in Mexico by Frank Por Laboratories S.A. de C.V.

Distributed by XXXXX

DRUG FACTS

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • On open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears and mouth. I case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash occurs. These may be signs of serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

SPL UNCLASSIFIED SECTION

  • Do not store above 105ºF (40ºC)
  • May discolor certain wood surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carbomer, C.I. 42090, Fragrance, Glycerin, Menthol, Triethanolamine, Water.

Questions or comments?

OTC - QUESTIONS SECTION

#-###-###-###

*Mix of moisturizers that will keep your hands moisturized for up to 24 hours.

Made in Mexico by Frank Por Laboratories S.A. de C.V.

Distributed by XXXXX

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BQ
Pharma
Hand
Sanitizer
70 % Ethyl Alcohol
3.04 fl oz.

PRINCIPAL DISPLAY PANEL BQ Pharma Hand Sanitizer 70 % Ethyl Alcohol 3.04 fl oz.PRINCIPAL DISPLAY PANEL BQ Pharma Hand Sanitizer 70 % Ethyl Alcohol 3.04 fl oz.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BQ
PHARMA
HAND
SANITIZER
70 % ETHYL ALCOHOL
13.52 fl Oz.

BQ PHARMA HAND SANITIZER 70 % ETHYL ALCOHOL 13.52 fl Oz.BQ PHARMA HAND SANITIZER 70 % ETHYL ALCOHOL 13.52 fl Oz.

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78817-001-012022-01-28C16284748780-1d6a99b39-631e-a426-e053-dadaa90af4c2BQ Pharma Hand Sanitizer 70 Percent
78817-001-022022-01-28C16284748780-1d6a99b39-631e-a426-e053-dadaa90af4c2BQ Pharma Hand Sanitizer 70 Percent
78817-001-032022-01-28C16284748780-1d6a99b39-631e-a426-e053-dadaa90af4c2BQ Pharma Hand Sanitizer 70 Percent
78817-001-042022-01-28C16284748780-1d6a99b39-631e-a426-e053-dadaa90af4c2BQ Pharma Hand Sanitizer 70 Percent
78817-001-052022-01-28C16284748780-1d6a99b39-631e-a426-e053-dadaa90af4c2BQ Pharma Hand Sanitizer 70 Percent
78817-001-062022-01-28C16284748780-1d6a99b39-631e-a426-e053-dadaa90af4c2BQ Pharma Hand Sanitizer 70 Percent
78817-002-032022-01-28C16284748780-1d6a99b39-631e-a426-e053-dadaa90af4c2BQ Pharma Hand Sanitizer 70 Percent
78817-002-042022-01-28C16284748780-1d6a99b39-631e-a426-e053-dadaa90af4c2BQ Pharma Hand Sanitizer 70 Percent
78817-002-052022-01-28C16284748780-1d6a99b39-631e-a426-e053-dadaa90af4c2BQ Pharma Hand Sanitizer 70 Percent
78817-002-062022-01-28C16284748780-1d6a99b39-631e-a426-e053-dadaa90af4c2BQ Pharma Hand Sanitizer 70 Percent

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78817-001-01BQ Pharma Hand Sanitizer90 mL in 1 BOTTLEGEL902
78817-001-02BQ Pharma Hand Sanitizer180 mL in 1 BOTTLEGEL1802
78817-001-03BQ Pharma Hand Sanitizer1000 mL in 1 BOTTLEGEL10002
78817-001-04BQ Pharma Hand Sanitizer400 mL in 1 BOTTLEGEL4002
78817-001-05BQ Pharma Hand Sanitizer400 mL in 1 BOTTLEGEL4002
78817-001-06BQ Pharma Hand Sanitizer500 mL in 1 BOTTLEGEL5002
78817-002-03BQ Pharma Hand SanitizerFresh Scent1000 mL in 1 BOTTLEGEL10002
78817-002-04BQ Pharma Hand SanitizerFresh Scent400 mL in 1 BOTTLEGEL4002
78817-002-05BQ Pharma Hand SanitizerFresh Scent400 mL in 1 BOTTLEGEL4002
78817-002-06BQ Pharma Hand SanitizerFresh Scent500 mL in 1 BOTTLEGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78817-001BQ PHARMA HAND SANITIZER (ALCOHOL) GEL BQ PHARMA HAND SANITIZER FRESH SCENT (ALCOHOL) GEL [FRANK POR LABORATORIES, S.A. DE C.V.]2Legacy NDC, 6 package rows20201009_65a1d6dc-3714-48c8-a814-d7f12df2560f.zip
78817-002BQ PHARMA HAND SANITIZER (ALCOHOL) GEL BQ PHARMA HAND SANITIZER FRESH SCENT (ALCOHOL) GEL [FRANK POR LABORATORIES, S.A. DE C.V.]2Legacy NDC, 4 package rows20201009_65a1d6dc-3714-48c8-a814-d7f12df2560f.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78817-00178817-001-01, 78817-001-02, 78817-001-03, 78817-001-04, 78817-001-05, 78817-001-06
78817-00278817-002-03, 78817-002-04, 78817-002-05, 78817-002-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
GLYCERINPDC6A3C0OXIACT
MENTHOLL7T10EIP3AIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
GLYCERINPDC6A3C0OXIACT
MENTHOLL7T10EIP3AIACT
TROLAMINE9O3K93S3TKIACT
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
677b83a5-38c8-4f05-8e9f-77cdfeb893be65a1d6dc-3714-48c8-a814-d7f12df2560f2020-08-25WarningsExact identifier
spl id: 677b83a5-38c8-4f05-8e9f-77cdfeb893be
spl set id: 65a1d6dc-3714-48c8-a814-d7f12df2560f

Reported adverse events (FAERS/openFDA)#

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