MENTHOL, CAMPHOR- menthol, camphor cream 
SUNSET PAIN RELIEF

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.

----------

72937-010-02
72937-010-04
72937-010-08
72937-010-16

Camphor 3%

Menthol 10%

​Topical Analgesic

USE

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

For external use only. · Ask a doctor before use if you have redness over affected area

Use only as directed.
Do not bandage tightly.
Do not use with heating pad, pack, wrap, hot water bottle or any heating element.
In case of accidental ingestion, contact doctor immediately.

If prone to allergic reaction to the product, consult to a doctor before using.

Condition worsens.
Redness is present.
Irritation develops.
Symptoms persist for more than 7 days or clear up occur again within a few days.

You experience signs injury, such as pain, swelling or blistering where the product was applied.

If pregnant or breast – feeding

Ask a health professional before use.

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

Directions

Adults and Children over 12 years

Apply a thin layer to the affected area and rub gently not more than 3 to 4 times a day.
Wash hands with soap and water after use.

Children under 12 years of age: do not use, consult a doctor.

Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

Water (Aqua), Paraffinum Liquidum, Alcohol Denat, Stearic Acid, Cetearyl Alcohol, Polysorbate 60, Cetyl
Alcohol, Dimethicone, Glyceryl Stearate, Glycereth-26, Tocopheryl Acetate, Propylene Glycol, Diazolidinyl
Urea, Methylparaben, Propylparaben, Cannabis Sativa Seed Oil, Stearyl Alcohol, Acrylamide/Sodium
Acrylate Copolymer, Trideceth-6, Polysorbate 20, Triethanolamine, Fragrance (Parfum), Sodium
Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract,
Hydroxyproline, Sodium Benzotriazolyl Butylphenol Sulfonate, Buteth-3, Tributyl Citrate, Cannabidiol,
FD&C Blue No.1 (CI 42090), Linalool, Limonene, Benzyl Benzoate, Coumarin, Geraniol.

SUNSET PAIN RELIEF CREAM GOLD 2 OZ

PAIN RELIEF CREAM 2

SUNSET PAIN RELIEF CREAM GOLD 4 OZ

PAIN RELIEF CREAM 4OZ

SUNSET PAIN RELIEF CREAM GOLD 8 OZ

PAIN RELIEF CREAM 8

SUNSET PAIN RELIEF CREAM GOLD 16 OZ

SUNSET PAIN RELIEF 16

MENTHOL, CAMPHOR 
menthol, camphor cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72937-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM10 g  in 100 g
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PANTHENOL (UNII: WV9CM0O67Z)  
ALCOHOL (UNII: 3K9958V90M)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIMETHICONE 1000 (UNII: MCU2324216)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
BENZYL BENZOATE (UNII: N863NB338G)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
GLYCERETH-26 (UNII: NNE56F2N14)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
TRIBUTYL CITRATE (UNII: 827D5B1B6S)  
GERANIOL (UNII: L837108USY)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
TROLAMINE (UNII: 9O3K93S3TK)  
HYDROXYPROLINE (UNII: RMB44WO89X)  
BUTETH-3 (UNII: OC116GRO69)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
COUMARIN (UNII: A4VZ22K1WT)  
CANNABIDIOL (UNII: 19GBJ60SN5)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)  
SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)  
WATER (UNII: 059QF0KO0R)  
MINERAL OIL (UNII: T5L8T28FGP)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72937-010-04113 g in 1 JAR; Type 0: Not a Combination Product09/15/2023
2NDC:72937-010-0257 g in 1 JAR; Type 0: Not a Combination Product09/15/2023
3NDC:72937-010-08227 g in 1 JAR; Type 0: Not a Combination Product09/15/2023
4NDC:72937-010-16454 g in 1 JAR; Type 0: Not a Combination Product09/15/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/24/2019
Labeler - SUNSET PAIN RELIEF (067218145)
Registrant - CHEMCO CORPORATIOM (032495954)

Revised: 9/2023
Document Id: 05b8c42f-48f8-62ea-e063-6394a90a8b32
Set id: 89f5f688-856f-f2df-e053-2995a90a73cf
Version: 20
Effective Time: 20230919
 
SUNSET PAIN RELIEF