INGROWN TOENAIL DROPS- chitosan oil

Ingrown Toenail Drops by

Drug Labeling and Warnings

Ingrown Toenail Drops by is a Otc medication manufactured, distributed, or labeled by Guangzhou Haishi Biological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

CHITOSAN 5%

ALLANTOIN 0.5%

Purpose

The nail care drops is an effectivesolution for ingrown nails byhelping you cure in growth, preventinflammation and relieve pain. Ltalso helps soften and lighten youringrown nails. Used 3-4 times aweek, in 2 to 4 weeks, the visibleeffect will appear.

Uses

Wash and dry nails thoroughly.Use the Lifter tool to gently removedirt along nail edgesApply 2-3 drops of solution to theaffected nail with the droppeg2-3times daily.Wear the toe cap for com fort andprotection.Continue for1-2veeksor until nails improve.

Warnings

For external use only.

Stop use and ask a doctor if

rash occurs.

Do not use

If pregnant or breast-feeding,ask adoctor before use

When using this product

keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Dosage

Apply 2-3 drops of solution to theaffected nail with the droppeg 2-3 times daily.

Inactive ingredients

WATER 53.15%
SALICYLIC ACID 2%
ANGELICA ARCHANGELICA EXTRACT 1%
TEA TREE LEAF OIL 1%
LACTIC ACID 2%
ALCOHOL 5%
SODIUM HYALURONATE 0.3%
BUTYLENE GLYCOL 3%
PROPYLENE GLYCOL 3%
GLYCERIN 3%
PANTHENOL 2%
DIPOTASSIUM GLYCYRRHIZATE 0.3%
BETAINE 1%
DISODIUM EDTA 0.05%
BETA-GLUCAN 2%
CENTELLA ASIATICA ROOT EXTRACT 2% CHRYSANTHELLUM INDICUM EXTRACT 2%
SOPHORA ANGUSTIFOLIA ROOT EXTRACT 2% PELARGONIUM GRAVEOLENS EXTRACT 2%
GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT 2%
PANAX GINSENG ROOT EXTRACT 2%
ASCORBIC ACID 2%
ARGININE 0.2%
HYDROXYACETOPHENONE 0.5%
1,2-HEXANEDIOL 0.5%
PENTYLENE GLYCOL 0.5%

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

INGROWN TOENAIL DROPS 
chitosan oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60771-0007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLIGLUSAM (UNII: 82LKS4QV2Y) (POLIGLUSAM - UNII:82LKS4QV2Y)	POLIGLUSAM	5 g  in 100 mL
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LACTIC ACID (UNII: 33X04XA5AT)
SALICYLIC ACID (UNII: O414PZ4LPZ)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60771-0007-1	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/07/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M029	12/07/2024

Labeler - Guangzhou Haishi Biological Technology Co., Ltd. (421262738)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Haishi Biological Technology Co., Ltd.		420929116	manufacture(60771-0007)