Clairfore

Manufacturer: ORGANELLE Inc
Effective date: 2020-10-31
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:32:43

Label at a glance#

ProductClairfore

Active ingredientASCORBIC ACID

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

L-ascorbic acid

INACTIVE INGREDIENT SECTION

Water, chitosan, egg white hydrolysate

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

OTC - PURPOSE SECTION

hand sanitizer to help reduce bacteria that potentially can cause disease

for use when soap and water are not available

INDICATIONS & USAGE SECTION

Place enough product on hands to cover all surfaces.Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

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

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
ASCORBIC ACID Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7	Product name	1	20171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75768-0002-1	2023-01-30	C162847	48780-1	f386c649-a740-0266-e053-dadaa90a7c1a	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75768-0002-1	Clairfore	100 mL in 1 BOTTLE	LIQUID	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75768-0002	CLAIRFORE (L-ASCORBIC ACID) LIQUID [ORGANELLE INC]	1	Legacy NDC, 1 package rows	20201101_b2feb130-81db-c141-e053-2a95a90a6c54.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Clairfore
L-ascorbic acid
ASCORBIC ACID
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75768-0002	75768-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ASCORBIC ACID	PQ6CK8PD0R	ACTIB
WATER	059QF0KO0R	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
b2feb28a-0d0f-c989-e053-2995a90a8eaa			b2feb130-81db-c141-e053-2a95a90a6c54	2020-10-31	Warnings	Exact identifier spl id: b2feb28a-0d0f-c989-e053-2995a90a8eaa spl set id: b2feb130-81db-c141-e053-2a95a90a6c54

Reported adverse events (FAERS/openFDA)#

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