FREEZIN COLD TOAST- methyl salicylate cream 
Q.A. Laboratories

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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Drug Facts

Active Ingredient  Purpose

Methyl salicylate 31% topical analgesic

Menthol 11% topical analgesic

USES temporarily relieves minor body aches and pains of muscle and joints associated with: simple backache

arthritis sprains bruises strains

Warnings for external use only

Do not use ¡ on wounds ¡ on damaged skin
¡ with a heating pad ¡ on a child under 12
years of age with arthritis-like conditions

Ask a doctor before use if you have
redness over the affected area.

When using this product ¡ avoid contact
with eyes and mucous membranes ¡ do
not bandage tightly

Stop use and ask doctor if ■ condition
worsens or symptoms persist for more than
7 days ■ symptoms clear up and occur within
a few days ■ excessive skin irritation occurs

Keep out of reach of children.
In case of accidental ingestion, get medical
help or contact a Poison Control Center right
away (1-800-222-1222)

Directions ¡ use only as directed
¡ adults and children 12 years of age
or older: apply to af fected area not more
than 3 to 4 times daily ¡ children under
12 years of age: ask a doctor

Other information
■ store between 20-25° C (68-77°F).
■ Protect from freezing

apply to affected area not more
than 3 to 4 times daily

Inactive ingredients
DEIONIZED WATER, CETEARYL ALCOHOL,
ISOPROPYL MYRISTATE, ISOCETYL STEARATE,
POLYSORBATE 60, SODIUM POLYACRYLOYLDIMETHYL
TAURATE, PHENOXYETHANOL,
HYDROGENATED POLYDECENE, CHAMOMILLA
RECUTITA (MATRICARIA) FLOWER EXTRACT,
METHYL PARABEN, TRIDECETH-10,
ROSMARINUS OFFICINALIS (ROSEMARY),
LEAF EXTRACT, FRANKINCENSE EXTRACT,
PROPYL PARABEN

Questions or comments:
1-800-4NO-PAIN,
toastproducts.com
MFD FOR: Toast Products
400 Sproul Street,
Pittsburgh, PA 15136
MFG IN USA

image of label

FREEZIN COLD TOAST 
methyl salicylate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52099-8000
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE31 g  in 100 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM11 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
ISOCETYL STEARATE (UNII: 3RJ7186O9W)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
HYDROGENATED POLYDECENE TYPE I (UNII: U333RI6EB7)  
MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
TRIDECETH-10 (UNII: G624N6MSBA)  
FRANKINCENSE (UNII: R9XLF1R1WM)  
ROSEMARY (UNII: IJ67X351P9)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52099-8000-1141 g in 1 TUBE; Type 0: Not a Combination Product06/12/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/12/2012
Labeler - Q.A. Laboratories (065361149)
Registrant - Q.A. Laboratories (065361149)
Establishment
NameAddressID/FEIBusiness Operations
Q.A. Laboratories065361149manufacture(52099-8000)

Revised: 1/2022
Document Id: 7cb8e2c4-61b8-400d-8e14-018a43ab5d45
Set id: 80e04a9a-202c-471d-9d76-c0b129cad24f
Version: 3
Effective Time: 20220117
 
Q.A. Laboratories