Beam Balm FUNGL NAIL by Jiangxi Hemei Pharmaceutical Co., Ltd 84010-191 complete

Beam Balm FUNGL NAIL by

Drug Labeling and Warnings

Beam Balm FUNGL NAIL by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BEAM BALM FUNGL NAIL- tolnaftate 1% fungl nail liquid 
Jiangxi Hemei Pharmaceutical Co., Ltd

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84010-191 complete

Active Ingredient

Tolnaftate 1%

Purpose

Antifungal

Use

Antifungal treatment for fingernails,toenails, and surrounding skin.Effective against fungal nails and athlete's foot caused by fungi.

Warnings

For external use only.

Do not use

if you experience any signs of sensitivity or irritation

When Using

Not for use in the eyes, mouthor vaginal area.

Stop Use

lf the area of application shows increased irritation lf there is Consult a doctor if symptoms worsen.If pregnant or breaslleeding

Ask Doctor

lf the area of application shows increased irritation lf there is Consult a doctor if symptoms worsen.If pregnant or breaslleeding

Keep Oot Of Reach Of Children

lf accidental ingestion occurs,seek medical assistance or contact a Poison Control Centerimmediately.

Directions

For athlete's foot and ring worm：use daily for 4 weeks.Clean the affected area and dry thoroughly.Keep away from fire and flames.For external use on nails and the immediately adjacent skin only.Use once daily, preferably before bedtime.
Unscrew the bottle cap and use the brush to apply the medicine directlyto the nail.The medication will then penetrate deeply into the nail.If the nail area is infected, spray the medication onto the affected area.SHAKE WELL BEFORE USE.Store at 5'c to 30°0(41'F to 86°F) in a cool dry place. Keep tighosedand away from sunlight.

Inactive ingredients

water ,euphorbia hirta whole, glycerin hydracrylic acid, pseudolarix amabilis bark, resorcinol.

PRINCIPAL DISPLAY PANEL

BEAM BALM FUNGL NAIL 
tolnaftate 1% fungl nail liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-191
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
RESORCINOL (UNII: YUL4LO94HK)
PSEUDOLARIX AMABILIS BARK (UNII: 49G13A93VE)
EUPHORBIA HIRTA WHOLE (UNII: L13YF113GN)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
HYDRACRYLIC ACID (UNII: C4ZF6XLD2X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-191-01	4 mL in 1 TUBE; Type 0: Not a Combination Product	09/29/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	09/29/2025	02/08/2026

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-191)

Revised: 2/2026

Document Id: 4a47b902-f3a6-9ff6-e063-6294a90af206

34390-5

Set id: 3fe89c8e-0c49-abb0-e063-6294a90a9710

Version: 2

Effective Time: 20260207