groovi beauty Rainbow Sprinkles Hand Sanitizer

Manufacturer: Ganzhou Olivee Cosmetic Co., Ltd.
Effective date: 2020-06-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:19:18

Label at a glance#

Productgroovi beauty Rainbow Sprinkles Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Rub dime sized amount between hands until dry Supervise children in the use of this product In case of eye contact, rinse eyes thoroughly with water

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 66%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help Decreases bacteria on the skin
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep product away from heat or flame.

Does not contain grain alcohol; do not drink, if taken internally will produce severe gastric disturbances.

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 redness develops and lasts.

Other information

Do not store above 105℉
May discolor some fabrics

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

Rub dime sized amount between hands until dry
Supervise children in the use of this product
In case of eye contact, rinse eyes thoroughly with water

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance, Water

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1039811	ethanol 66 % Topical Gel	PSN	1
1039811	ethanol 0.66 ML/ML Topical Gel	SCD	1
1039811	ethanol 66 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
56136-348-01	2025-01-30	C162847	48780-1	2cef2736-9079-d83d-e063-dadaa90ab31f	HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
56136-348-01	groovi beauty Rainbow Sprinkles 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
56136-348	GROOVI BEAUTY RAINBOW SPRINKLES HAND SANITIZER (ALCOHOL) GEL [GANZHOU OLIVEE COSMETIC CO., LTD.]	1	Legacy NDC, 1 package rows	20200627_bc5a751d-b438-4e2a-90f2-d87fb5b06020.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

groovi beauty Rainbow Sprinkles Hand Sanitizer
Alcohol
WATER
CARBOMER COPOLYMER TYPE A
AMINOMETHYLPROPANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
56136-348	56136-348-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
CARBOMER COPOLYMER TYPE A	71DD5V995L	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	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
8808644d-5d75-4479-9676-1752483c5409			bc5a751d-b438-4e2a-90f2-d87fb5b06020	2020-06-27	Warnings	Exact identifier spl id: 8808644d-5d75-4479-9676-1752483c5409 spl set id: bc5a751d-b438-4e2a-90f2-d87fb5b06020

Reported adverse events (FAERS/openFDA)#

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