EXTERNAL ANALGESIC- camphor, capsicum, menthol patch 
Hmong 21

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EXTERNAL ANALGESIC

Active ingredients

Camphor 9.6%

Capsaicin 0.05%

Menthol 7.8%

Purpose

External Analgesic

Uses

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

-simple backache

-arthritis

-strains

-bruises

-sprains

Warnings

When using this product

-avoid contact with the eyes

- do not apply to wounds or damaged skin

-do not bandage tightly

Stop use and ask a doctor if

- condition worsens

-if synthoms oersust for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding, 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.

Directions

Adults and children 12 years of age and older:

-Clean and dry affected area.

-Remove from backing film and apply.

-Remove from the skin after at most 8 hours' application.

-Apply to the affected area not more than 3 times daily.

-Children under 12 years of age: Consult a doctor.

Inactive ingredients

Acrylic Acid, Aluminum Hydroxide, Carmellose Sodium, 2-ethylhexylacrylate, Glycerin, Methyl Acrylate, Polyacrylate, polyacrylic Acid, sodium polyacrylatem, Tartaric Acid, Water.

Label

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EXTERNAL ANALGESIC 
camphor, capsicum, menthol patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70927-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)96 mg  in 1 g
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.5 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL78 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYL ACRYLATE (UNII: WC487PR91H)  
TARTARIC ACID (UNII: W4888I119H)  
WATER (UNII: 059QF0KO0R)  
CAPSICUM (UNII: 00UK7646FG)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70927-001-004 g in 1 PATCH; Type 0: Not a Combination Product08/25/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01708/25/2016
Labeler - Hmong 21 (080352437)

Revised: 12/2023
Document Id: 0d774b08-e5e4-56c9-e063-6294a90ae8db
Set id: 3b6155a5-51aa-2780-e054-00144ff8d46c
Version: 5
Effective Time: 20231226
 
Hmong 21