FAST RELIEF REUMACETIN- methyl salicylate and menthol cream 
Chemco Corporation

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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FAST RELIEF REUMACETIN

DRUG FACTS

Active Ingredient:                             Purpose:

Methyl Salicylate 12.5%......................External Analgesic

Menthol 2.5%.................................External Analgesic

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, sprains.

Warnings:

Keep out of reach of children to avoid accidental poisoning.

Caution: Discontinue use if excessive irritation of the skin develops. Avoid getting into eyes or mucous membranes. If condition worsens, or symptoms persist for more than 7 days or clear up and occur again within a few days, or redness is present, or in conditions affecting children under 12 years of age, discontinue use and consult a physician immediately.

Directions

Use as directed. Adults and children 12 years of age and older. Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age: consult a doctor.

Inactive Ingredients:

AQUA, PARAFFINUM LIQUIDUM, STEARIC ACID, GLYCERYL MONOSTEARATE, CETYL ALCOHOL, DIMETHICONE, GLYCERETH-26, PROPYLENE GLYCOL, DIAZOLIDINYL UREA, METHYLPARABEN, PROPYLPARABEN, STEARYL ALCOHOL, TRIETHANOLAMINE, ACRYLAMIDE, SODIUM ACRYLATE, TRIDECETH-6, SODIUM HYALURONATE, SODIUM PCA, WHEAT AMINO ACIDS, PANTHENOL, SYMPHYTUM OFFICINALE EXTRACT, HYDROXYPROLINE.

Manufactured by:

Chemco Corp.

Miami, FL 33014.

FAST RELIEF

REUMACETIN

For Muscle Ache & Arthritis Pain!

Greaseless

Stainless

Long Lasting Cream

Net Wt 8 oz (226g)

Made in USA

image description

FAST RELIEF REUMACETIN 
menthol, methyl salicylate cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49283-006
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 12.5 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2.5 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
MINERAL OIL (UNII: T5L8T28FGP)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERETH-26 (UNII: NNE56F2N14)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
TROLAMINE (UNII: 9O3K93S3TK)  
ACRYLAMIDE (UNII: 20R035KLCI)  
SODIUM ACRYLATE (UNII: 7C98FKB43H)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
PANTHENOL (UNII: WV9CM0O67Z)  
COMFREY LEAF (UNII: DG4F8T839X)  
HYDROXYPROLINE (UNII: RMB44WO89X)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49283-006-08 226 g in 1 JAR
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 08/26/2013
Labeler - Chemco Corporation (032495954)
Registrant - Chemco Corporation (032495954)
Establishment
Name Address ID/FEI Business Operations
Chemco Corporation 032495954 manufacture(49283-006)

Revised: 12/2014
Document Id: e54e85df-63d5-4a0c-b3bd-19d17c0605d5
Set id: 188e0cb8-d1a9-4e30-ae47-f6db16c420ed
Version: 3
Effective Time: 20141222
 
Chemco Corporation