Smart Care Marvel Hand Sanitizer

Manufacturer: Ashtel Studios, Inc
Effective date: 2020-08-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:26:09

Label at a glance#

ProductSmart Care Marvel Hand Sanitizer

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

• Put a thumbnail size amount in your palm and rub your hands together briskly until dry. • Children under 6 years of age should be supervised when using this product. • Not recommended for infants.

Storage and handling

• Do not store above 100˚F (38˚C). • May discolor some fabrics. • Harmful to wood finishes & plastics.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

• To help reduce bacteria and germs on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable.

• Keep away from fire or flame.

When using this product

• Keep out of eyes.

• Do not inhale or ingest.

• In case of contact with eyes, flush thoroughly with water.

• Avoid contact with broken skin.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• Put a thumbnail size amount in your palm and rub your hands together briskly until dry.

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

• Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

• Do not store above 100˚F (38˚C).

• May discolor some fabrics.

• Harmful to wood finishes & plastics.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water, Carbomer, Fragrance, Aminomethyl Propanol, Denatonium Benzoate, *Blue 1(CI 42090), *Red 4(CI 14700), *Red 33(CI 17200), *Yellow

5(CI 19140). *Contains one or more of these ingredients.

Questions?

OTC - QUESTIONS SECTION

(909)434-0911

SPL UNCLASSIFIED SECTION

KILLS 99% OF MOST COMMON GERMS

DESIGNED IN U.S.A.

MADE IN CHINA

PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

DISTRIBUTED BY

ASHTEL STUDIOS INC.

ONTARIO, CA 91761

Smart Care*

SMARTCAREUS.COM

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Packaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	1
581660	ethanol 0.62 ML/ML Topical Gel	SCD	1
581660	ethanol 62 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70108-067-01	2024-01-30	C162847	48780-1	1030e365-3b71-111a-e063-dadaa90a10e2	MARVEL Smart Care* HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70108-067-01	Smart Care Marvel Hand Sanitizer	29 mL in 1 BOTTLE	GEL	29		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70108-067	SMART CARE MARVEL HAND SANITIZER (ETHYL ALCOHOL) GEL [ASHTEL STUDIOS, INC]	1	Legacy NDC, 1 package rows	20200829_1a8144c7-8d29-44ed-a6cb-5ff3b159c722.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Smart Care Marvel Hand Sanitizer
Ethyl alcohol
ALCOHOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
AMINOMETHYLPROPANOL
DENATONIUM BENZOATE
FD&C BLUE NO. 1
FD&C RED NO. 4
D&C RED NO. 33
FD&C YELLOW NO. 5

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70108-067	70108-067-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
DENATONIUM BENZOATE	4YK5Z54AT2	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
FD&C RED NO. 4	X3W0AM1JLX	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
FD&C YELLOW NO. 5	I753WB2F1M	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
90a78b50-7d68-441b-a7a4-76eb362c602a			1a8144c7-8d29-44ed-a6cb-5ff3b159c722	2020-08-24	Warnings	Exact identifier spl id: 90a78b50-7d68-441b-a7a4-76eb362c602a spl set id: 1a8144c7-8d29-44ed-a6cb-5ff3b159c722

Reported adverse events (FAERS/openFDA)#

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