BEAMBALM ANTIFUNGAL FOOT SOAKING PACK- zinc undecylenate 5% antifungal foot soaking pack powder

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

ZINC UNDECYLENATE 5%

Purpose

ANTI-FUNGAL

Use

FOR THE TREATMENT OF MOST ATHLETE'S FOOT (TINEA PEDIS), JOCK ITCH (TINEA CRURIS) AND RINGWORM (TINEA CORPORIS).
FOR EFFECTIVE RELIEF OF ITCHING, CRACKING, BURNING, REDNESS, SORENESS, IRRITATION AND DISCOMFORT

Warnings

FOR EXTERNAL USE ONLY
DO NOT APPLY TO WOUNDS OR DAMAGED SKIN
IF PREGNANT OR BREAST FEEDING, ASK A HEALTH PROFESSIONAL BEFORE USE.
DO NOT USE ON CHILDREN UNDER 2 YEARS OF AGE UNLESS DIRECTED BY A DOCTOR.

Do not use

DO NOT USE ON CHILDREN UNDER 2 YEARS OF AGE UNLESS DIRECTED BY A DOCTOR.

When Using

WHEN USING THIS PRODUCT AVOID CONTACT WITH THE EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.

Stop Use

IF YOU EXPERIENCE ANY IRRITATION OR DISCOMFORT, PLEASE STOP USING IT AND CONSULT A DOCTOR.

Ask Doctor

IF YOU EXPERIENCE ANY IRRITATION OR DISCOMFORT, PLEASE STOP USING IT AND CONSULT A DOCTOR.

Keep Out Of Reach Of Children

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

Directions

FILL THE FOOT BASIN WITH WARM WATER AND ADD 2-3 PACKS OF FOOT BATH BAGS TO IT. SOAK YOUR FEET IN IT FOR 30 MINUTES ONCE A DAY. IF YOU WANT TO ENHANCE THE EFFECT

Inactive ingredients

TALCUM POWDER, MUGWORT, SILICON DIOXIDE, SOPHORA FLAVESCENS

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BEAMBALM ANTIFUNGAL FOOT SOAKING PACK 
zinc undecylenate 5% antifungal foot soaking pack powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-192
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC UNDECYLENATE (UNII: 388VZ25DUR) (UNDECYLENIC ACID - UNII:K3D86KJ24N)	ZINC UNDECYLENATE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ARTEMISIA LUDOVICIANA WHOLE (UNII: A9RC4Q0VLW)
TALC (UNII: 7SEV7J4R1U)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-192-01	20 in 1 BAG	04/22/2026
1		5 g in 1 BAG; 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	04/22/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Zhongletang Pharmaceuticals Co.,Ltd.		411295811	manufacture(85248-192)