NOORISH FOOT CO. ANTI-FUNGAL PEN- anti-fungal pen liquid

Noorish Foot Co. Anti-Fungal Pen by

Drug Labeling and Warnings

Noorish Foot Co. Anti-Fungal Pen by is a Otc medication manufactured, distributed, or labeled by Guangzhou Mizi Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Undecylenic Acid 10%........ Anti-Fungal

Purpose

Anti-Fungal

Use

Cures most athlete's foot (dermatophytosis).
Relieves itching, scaling and

Warnings

For external use only

Do not use on children under 2 years

for diaper rash

When using this product Avoid contact with the eyes

Stop use and consult a doctor if

irritation occurs if there is no improvement within 4 weeks

KEEP OUT OF REACH OF CHILDREN

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

Directions

Wash the affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Supervise children in the use of this product. For athlete's foot: Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily For athlete's foot and ringworm, use daily for 4 weeks. If condition persists longer, consult a doctor.

Other information

Store at room temperature 15°-30°C (59°-86°F).

Inactive ingredients

Biotin, Deacetylated Chitin, Disodium EDTA,

Ethanol, Glycerol, Keratin, Lactic Acid,

PCA Calcium, Propylene Glycol, Retinol, Salicylic Acid, Sorbitol, Urea,

Vitamin E, Water.

Package Label - Principal Display Panel

5 mL: NDC: 84896-111-11

INGREDIENTS AND APPEARANCE

NOORISH FOOT CO. ANTI-FUNGAL PEN 
anti-fungal pen liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84896-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
UNDECYLENIC ACID (UNII: K3D86KJ24N) (UNDECYLENIC ACID - UNII:K3D86KJ24N)	UNDECYLENIC ACID	10 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)
SALICYLIC ACID (UNII: O414PZ4LPZ)
GLYCERIN (UNII: PDC6A3C0OX)
LACTIC ACID (UNII: 33X04XA5AT)
SORBITOL (UNII: 506T60A25R)
CHITIN (UNII: 8SH93A7QWW)
UREA (UNII: 8W8T17847W)
RETINOL (UNII: G2SH0XKK91)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ACETALDEHYDE (UNII: GO1N1ZPR3B)
CALCIUM PCA (UNII: 7Y2LVU5EKK)
BIOTIN (UNII: 6SO6U10H04)
KERATIN, TYPE I CYTOSKELETAL 18 (UNII: ZS6J3E8DAS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84896-111-11	2 in 1 BOX	01/01/2025
1		5 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	01/01/2025

Labeler - Guangzhou Mizi Biotechnology Co., Ltd. (418001649)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Mizi Biotechnology Co., Ltd.		418001649	manufacture(84896-111)