CT Cosmetics Co., Ltd - Hug Lets CC Hand Sanitizer Gel(Ethanol)

Manufacturer: Purgofarm Co Ltd
Effective date: 2020-04-25
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:08:01

Label at a glance#

ProductPURISTIC

Active ingredientSODIUM CHLORITE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sodium chlorite

INACTIVE INGREDIENT SECTION

water, citric acid

OTC - PURPOSE SECTION

■ remove 99.9% of viruses, bacteria & fungi

■ deodorizes the immediate area round it

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

■ tap lightly downward, gently bend the dot of ampoule

■ content turn yellow, to activate and emit through the body surface

■ content turn white, to be discarded in regular trash

WARNINGS SECTION

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

Do not use

in children less than 2 months of age
on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76648-0001-1	2023-01-30	C162847	48780-1	f386c649-c134-0266-e053-dadaa90a7c1a	CT Cosmetics Co., Ltd - Hug Lets CC Hand Sanitizer Gel(Ethanol)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76648-0001-1	PURISTIC	6 mL in 1 SYRINGE, PLASTIC	LIQUID	6		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76648-0001	PURISTIC (SODIUM CHLORITE) LIQUID [PURGOFARM CO LTD]	1	Legacy NDC, 1 package rows	20200426_a41dd3c6-31cf-c49c-e053-2a95a90aec50.zip

Products#

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

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

PURISTIC
SODIUM CHLORITE
WATER
CHLORITE ION
CITRIC ACID ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76648-0001	76648-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM CHLORITE	G538EBV4VF	ACTIB
CITRIC ACID ACETATE	DSO12WL7AU	IACT

Source Document#

Source XML · Source PDF

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
a41dd403-f62c-6538-e053-2995a90a0be5			a41dd3c6-31cf-c49c-e053-2a95a90aec50	2020-04-25	Warnings	Exact identifier spl id: a41dd403-f62c-6538-e053-2995a90a0be5 spl set id: a41dd3c6-31cf-c49c-e053-2a95a90aec50

Reported adverse events (FAERS/openFDA)#

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