KUNG FU PATCH ™ - PAIN RELIEF PATCH

KUNG FU PAIN RELIEF by

Drug Labeling and Warnings

KUNG FU PAIN RELIEF by is a Otc medication manufactured, distributed, or labeled by 6c23, Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KUNG FU PAIN RELIEF- menthol, methyl salicylate patch 
6c23, Llc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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KUNG FU PATCH ™ - PAIN RELIEF PATCH

Drug Facts

Active ingredients

Menthol 2%

Methyl Salicylate 0.5%

Purpose

Topical analgesic

Uses

For temporary relief of minor aches and pains of  muscles and joints associated with

● simple backache ● strains ● sprains ● arthritis ● bruises 

Warnings

For external use only

Do not use

● on the face ● on wounds or damaged skin or irritated skin ● with heating pad or device ● with, or at the same time as, other external analgesic products ● right before or after heart surgery

Ask a doctor before use if

● you are prone to allergic reaction ● you are allergic to topical products

When using this product

avoid contact with eyes, mucous membranes or rashes ● do not bandage tightly ● do not use otherwise than directed

Stop use and ask a doctor if

Condition worsens ● if symptoms persist for more than 7 days or clear up occur again within a few days ● rash, itching or excessive skin irritation develops

If pregnant or breast-feeding, ask a health professional before use while breast-feeding and during the first 6 months of pregnancy. Do not use during the last 3 months of pregnancy because it may cause problems in the unborn child or complications during delivery. Or ask a health professional before use.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away. Package not child resistant.

Directions

Adults and children 2 years of age and older: ● clean and dry affected area ● remove patch from film ● apply to affected area not more than 2 times daily for 3 days ● remove patch from skin after at most 8 hours of application ● do not use more than 3 patches per day ● the used patch should be removed from the skin when a new one is applied.

Children under 2 years of age: do not use

Inactive ingredients

Acanthopanacis Cortex, Aconiti Lateralis Radix, Acori Graminei Rhizoma, Angelica Sinensis Radix, Atractylodis Rhizoma, Aucklandiae Radix, Borneolum, Carthami Flos, Cervi Cornu Pantotrichum, Chuanxiong Rhizoma, Cinnamomi Cortex, Cnidii Fructus, Cyathulae Radix, Dendrobii Caulis, Dioscoreae Hypoglaucae Rhizoma, Draconis Sanguis, Drynariae Rhizoma, FD&C Blue No. 2 (Indigotine), FD&C Yellow 5 (Tartrazine), Gentianae Macrophyllae Radix, Myrrha, Olibanum, Paeoniae Rubra Radix, Pinelliae Rhizoma, Pyritum, Resina Liquidambaris, Natural Resin, Rose Oil, Sesame Oil, Zinc Oxide

Other information

● store at 15°C to 30°C (59°F to 86°F) with lid closed tightly ● avoid storing product in direct sunlight ● protect product from excessive moisture

Questions or comments?

1-808-258-5198

Monday-Friday 9 a.m. - 5 p.m. HST
You may also report serious side effects to above phone number

The Newest Advanced Ancient Patch Technology
For temporary relief of pains
► Backache, Arthritis, Bruises, Strains & Sprains
► Works where pain is
► Convenient and not messy
► Flexes as you move
► Apply for 8-12 hours

5 patches, 4.5 g Each
3-15/16” X 6-1/10” (10cm X 15.5cm)

~Discard unused patches 3 weeks after opening ~

Package not child resistant. Keep out reach of children

Manufactured by
Hua Chang Biopharm Co., Ltd.
43, Chenggong Street, Gantian District, Tainan, 72046, Taiwan (R.O.C.)

Distributed by:
6C23 LLC. (Aiea Medical Building)
99-128 Aiea Heights Drive, #109, Aiea, HI 96701, U.S.A.
1(808)258-5198 | www.6c23.com

Made in Taiwan

Packaging

image description

KUNG FU PAIN RELIEF 
menthol, methyl salicylate patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 70467-812
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM2 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ELEUTHEROCOCCUS NODIFLORUS ROOT BARK (UNII: W7PRK433YB)  
ACONITUM CARMICHAELII LATERAL ROOT (UNII: 2A9PW94VJX)  
ACORUS GRAMINEUS ROOT (UNII: Z60N6Q6E19)  
ANGELICA SINENSIS ROOT (UNII: B66F4574UG)  
ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)  
AUCKLANDIA COSTUS ROOT (UNII: RUP970CGR9)  
BORNEOL (UNII: M89NIB437X)  
SAFFLOWER (UNII: 4VBL71TY4Y)  
CERVUS ELAPHUS HORN (UNII: 8H4VM8NQA5)  
LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT (UNII: RR83T99U97)  
CINNAMON (UNII: 5S29HWU6QB)  
CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)  
CYATHULA OFFICINALIS ROOT (UNII: BRM37UP34O)  
DENDROBIUM NOBILE STEM (UNII: CGO90PC910)  
TOKORO YAM (UNII: N57RVD5L6U)  
DRAGON'S BLOOD (UNII: M3YJ2C28IC)  
DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q)  
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
GENTIANA MACROPHYLLA ROOT (UNII: 6559FC0U1B)  
MYRRH (UNII: JC71GJ1F3L)  
FRANKINCENSE (UNII: R9XLF1R1WM)  
PAEONIA VEITCHII ROOT (UNII: VX6GD6M93V)  
PINELLIA TERNATA ROOT (UNII: G9AET085M5)  
FERROUS SULFIDE (UNII: TH5J4TUX6S)  
LIQUIDAMBAR FORMOSANA RESIN (UNII: 597LBL467J)  
PINE TAR (UNII: YFH4WC535J)  
ROSE OIL (UNII: WUB68Y35M7)  
SESAME OIL (UNII: QX10HYY4QV)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 70467-812-011 in 1 PACKAGE03/09/201712/31/2019
10.1125 g in 1 PATCH; Type 0: Not a Combination Product
2NDC: 70467-812-055 in 1 PACKAGE03/09/201712/31/2019
20.1125 g in 1 PATCH; Type 0: Not a Combination Product
3NDC: 70467-812-1010 in 1 PACKAGE03/09/201712/31/2019
30.1125 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/09/201712/31/2019
Labeler - 6c23, Llc (079988386)

Revised: 1/2020
 
6c23, Llc