My Little Pony Hand Sanitizer

Manufacturer: K7 Design Group Inc.
Effective date: 2020-12-11
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:35:06

Label at a glance#

ProductMy Little Pony Hand Sanitizer

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 69% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hand-washing to decrease bacteria on the skin, only when water is not available

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire and flames

When using this product

OTC - WHEN USING SECTION

do not get into eyes.
if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop

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

wet hands thoroughly with product and allow to dry without wiping

Other information

OTHER SAFETY INFORMATION

Store at 68F to 77F (20C - 25C)
Do not store above 110F (43C)
You may report a serious adverse reaction to this product to Report Reaction, LLC, PO Box 22, Plainsboro, NJ 08536

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Carbomer, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Fragrance, Tocopheryl Acetate, Denatonium Benzoate, Red 33, Blue 1.

Product Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MLP 200

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2287763	ethanol 69 % Topical Gel	PSN	1
2287763	ethanol 0.69 ML/ML Topical Gel	SCD	1
2287763	ethanol 69 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74177-957-01	2022-01-28	C162847	48780-1	d6a99b39-b56d-a426-e053-dadaa90af4c2	My Little Pony Hand Sanitizer Kit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74177-957-01	My Little Pony Hand Sanitizer	1 in 1 KIT	KIT	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74177-957	MY LITTLE PONY HAND SANITIZER (ALCOHOL) KIT [K7 DESIGN GROUP INC.]	1	Legacy NDC, 1 package rows	20201212_b634537f-ef69-c2fc-e053-2a95a90a3fde.zip

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

My Little Pony Hand Sanitizer
Alcohol
Bubblegum Scent Hand Soap
METHYLISOTHIAZOLINONE
FD&C BLUE NO. 1
METHYLCHLOROISOTHIAZOLINONE
WATER
SODIUM LAURETH SULFATE
SODIUM COCOYL GLYCINATE
EDETATE DISODIUM
COCAMIDOPROPYL BETAINE
SODIUM CHLORIDE
CITRIC ACID MONOHYDRATE
Berry Blast Scent Hand Sanitizer
.ALPHA.-TOCOPHEROL ACETATE
GLYCERIN
ALOE VERA LEAF
DENATONIUM BENZOATE
D&C RED NO. 33
PROPYLENE GLYCOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
AMINOMETHYLPROPANOL
Cherry Lip Balm
ETHYLHEXYL PALMITATE
SACCHARIN SODIUM
PHENOXYETHANOL
POLYISOBUTYLENE (1000 MW)
SQUALANE
CERESIN
YELLOW WAX

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74177-957	74177-957-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
METHYLISOTHIAZOLINONE	229D0E1QFA	INGR
FD&C BLUE NO. 1	H3R47K3TBD	INGR
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	INGR
WATER	059QF0KO0R	INGR
SODIUM LAURETH SULFATE	BPV390UAP0	INGR
SODIUM COCOYL GLYCINATE	XLU9KH03XM	INGR
EDETATE DISODIUM	7FLD91C86K	INGR
COCAMIDOPROPYL BETAINE	5OCF3O11KX	INGR
SODIUM CHLORIDE	451W47IQ8X	INGR
CITRIC ACID MONOHYDRATE	2968PHW8QP	INGR
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
DENATONIUM BENZOATE	4YK5Z54AT2	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
ETHYLHEXYL PALMITATE	2865993309	INGR
SACCHARIN SODIUM	SB8ZUX40TY	INGR
PHENOXYETHANOL	HIE492ZZ3T	INGR
POLYISOBUTYLENE (1000 MW)	5XB3A63Y52	INGR
SQUALANE	GW89575KF9	INGR
CERESIN	Q1LS2UJO3A	INGR
YELLOW WAX	2ZA36H0S2V	INGR

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
b6345239-9013-a206-e053-2a95a90a0122			b634537f-ef69-c2fc-e053-2a95a90a3fde	2020-12-11	Warnings	Exact identifier spl id: b6345239-9013-a206-e053-2a95a90a0122 spl set id: b634537f-ef69-c2fc-e053-2a95a90a3fde

Reported adverse events (FAERS/openFDA)#

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