SANMO-BL

Manufacturer
Beacon Promotions, Inc.
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:32:26

Label at a glance#

ProductSANMO-BL
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Directions ■ Put enough product in your palm to cover your hands and rub together briskly until dry ■ Children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

Drug Facts

DOSAGE & ADMINISTRATION SECTION

Ethyl alcohol 63.5%

Put enough product in your palm to cover your hands and rub together briskly until dry

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on the skin

Warnings

WARNINGS SECTION

Warnings
Flammable. Keep away from fire or flame.

■ 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 a doctor if irritation or rash appears and lasts.

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

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Directions

INSTRUCTIONS FOR USE SECTION

Directions

■ Put enough product in your palm to cover your hands and rub together briskly until dry

■ Children under 6 years of age should be supervised when using this product

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 63.5% w/w

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients: Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer Hydroxypropyl Methylcellulose, Mannitol, Microcrystalline Cellulose, Parfum, Propylene Glycol, Purified Water, Tocopheryl Acetate

Other

OTHER SAFETY INFORMATION

■ Store at room temperature

■ May discolor certain fabrics or surfaces

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CI1CI1

LBLB

SSSS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2003712ethanol 63.5 % Topical GelPSN2
2003712ethanol 0.635 ML/ML Topical GelSCD2
2003712ethanol 63.5 % Topical GelSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70445-607-01SANMO-BL15 mL in 1 BOTTLE, PLASTICGEL152
70445-607-02SANMO-BL30 mL in 1 BOTTLE, PLASTICGEL302
70445-607-03SANMO-BL60 mL in 1 BOTTLE, PLASTICGEL602
70445-607-04SANMO-BL120 mL in 1 BOTTLE, PLASTICGEL1202
70445-607-05SANMO-BL240 mL in 1 BOTTLE, PLASTICGEL2402
70445-607-06SANMO-BL240 mL in 1 BOTTLE, PUMPGEL2402
70445-607-07SANMO-BL300 mL in 1 BOTTLE, PUMPGEL3002
70445-607-08SANMO-BL480 mL in 1 BOTTLE, PLASTICGEL4802
70445-607-09SANMO-BL480 mL in 1 BOTTLE, PUMPGEL4802

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
SANMO-BLMOISTURIZING SANITIZER WITH BLUE BEADSBeacon Promotions, Inc.1eb96fb8-d750-9241-e063-6394a90a1cdd2026-01-12WarningsExact identifier
ndc (package): 70445-607-05
ndc (package): 70445-607-08
ndc (package): 70445-607-02
ndc (package): 70445-607-04
ndc (package): 70445-607-09
ndc (package): 70445-607-07
ndc (package): 70445-607-03
ndc (package): 70445-607-06
ndc (package): 70445-607-01
ndc (product): 70445-607
ndc11 (package): 70445060706
ndc11 (package): 70445060709
ndc11 (package): 70445060707
ndc11 (package): 70445060704
ndc11 (package): 70445060702
ndc11 (package): 70445060703
ndc11 (package): 70445060701
ndc11 (package): 70445060708
ndc11 (package): 70445060705
spl id: 48390ab4-8575-bac5-e063-6394a90ae1e4
spl set id: 1eb96fb8-d750-9241-e063-6394a90a1cdd

Reported adverse events (FAERS/openFDA)#

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