Bai Healing Cold Patch

Manufacturer
Sinopharm Group Dezhong (Foshan) Pharmaceutical Co., Ltd
Effective date
2020-12-04
Label type
HUMAN OTC DRUG LABEL
Version
32705
Source
legacy-cache
Hydrated at
2026-08-01 23:04:04

Label at a glance#

ProductBai Healing Cold Patch
Active ingredientMENTHOL
Label structure15 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains, sprains and bruises.

Dosage and administration

Adults (12 years and older) - Clean and dry the affected area. - Peel film off from patch and apply the herbal formula side onto skin. - Lasts for up to 24 hours; repeat as necessary and no less than 2 hours between applications. - For the best result, a 2-week course of treatment is recommended. - Children under 12 years: Consult your physician.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol     4.62%

Purpose

OTC - PURPOSE SECTION

Menthol           Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains, sprains and bruises.

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY. This product contains latex.

Ask a Doctor or Pharmacist Before Use If You Are

OTC - ASK DOCTOR/PHARMACIST SECTION

pregnant.
lactating women.

When Using This Product

OTC - WHEN USING SECTION

Do not apply to wounds or damaged, broken or irritated skin.

Stop Use and Ask a Doctor If

OTC - STOP USE SECTION

condition worsens.
redness is present.
irritation develops.
symptoms persist for more than 7 days or clear up and occur again within a few days.

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Adults (12 years and older)
- Clean and dry the affected area.
- Peel film off from patch and apply the herbal formula side onto skin.
- Lasts for up to 24 hours; repeat as necessary and no less than 2 hours between applications.
- For the best result, a 2-week course of treatment is recommended.
- Children under 12 years: Consult your physician.

Other Information

OTHER SAFETY INFORMATION

Keep pouch sealed and avoid storage in direct sunlight.

Questions or Comments?

OTC - QUESTIONS SECTION

1118 Cleghorn Dr. #E Diamond Bar, CA 91765
Tel: 323-859-1307

Manufactured by

SPL UNCLASSIFIED SECTION

Sinopharm Group Dezhong (Foshan) Pharmaceutical Co., Ltd
No. 89 Foping Road, Chanchang District, Foshan, Guangdong, China

Made in China

U.S. Distributor

SPL UNCLASSIFIED SECTION

Bai Healing LLC
Add: 1118 Cleghorn Dr. #E Diamond Bar, CA 91765

Inactive Ingredients

INACTIVE INGREDIENT SECTION

NOTOPTERYGIUM INCISUM ROOT, ANGELICA BISERRATA ROOT, ANGELICA DAHURICA ROOT, DRAGON'S BLOOD, CORYDALIS YANHUSUO TUBER, TETRAPANAX PAPYRIFER STEM, SAFFLOWER, EVODIAMINE, NATURAL LATEX RUBBER

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72479-32572479-325-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
42a69b5b-ad01-4ff7-94ec-5aefc5e2ca130b4a74e2-99fa-4a5a-bdc3-c4840f39ba9a2021-12-16WarningsExact identifier
spl set id: 0b4a74e2-99fa-4a5a-bdc3-c4840f39ba9a

Reported adverse events (FAERS/openFDA)#

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