INSTANT THERAPY- camphor (synthetic), menthol, unspecified form cream
Hampshire Laboratories Inc

----------

Instant Therapy

Drug Facts

Active ingredients

Camphor 3.1%

Menthol 1.3%

Purpose

Topical Analgesic

Indications

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

Warnings

• For external use only.
• Avoid contact with eyes.
• If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

• If swallowed, consult physician.

Do not apply to

• wounds or damaged skin.
• Do not bandage tightly.

If pregnant or breast feeding,

contact physician prior to use.

Directions

• Adults and children two years of age or older: Apply to affected area not more than three to four times daily.
• Children under two years of age: consult a physician.

Additional Information

Store at room temperature.

Inactive ingredients

Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water), BHT, Cetyl Alcohol, Cinnamomum Cassia (Cassia) Leaf Oil, Copper Sulfate, Diazolidinyl Urea, Eucalyptus Globulus Oil, Glyceryl Stearate, Methyl Paraben, PEG-100 Stearate, Polysorbate-20, Propyl Paraben, Propylene Glycol, Stearic Acid, Tocopheryl Acetate (Vitamin E), Triethanolamine, FD&C Blue #1.

Package Labeling:

Tube

INSTANT THERAPY
camphor (synthetic), menthol, unspecified form cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71423-825
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	31 mg in 1 mL
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	13 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CETYL ALCOHOL (UNII: 936JST6JCN)
CHINESE CINNAMON LEAF OIL (UNII: 4U4V2F2E4Y)
CUPRIC SULFATE (UNII: LRX7AJ16DT)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
EUCALYPTUS OIL (UNII: 2R04ONI662)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
METHYLPARABEN (UNII: A2I8C7HI9T)
PEG-100 STEARATE (UNII: YD01N1999R)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
STEARIC ACID (UNII: 4ELV7Z65AP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71423-825-01	75 mL in 1 TUBE; Type 0: Not a Combination Product	05/09/2017	06/08/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	05/09/2017	06/08/2020

Labeler - Hampshire Laboratories Inc (160736109)

Revised: 10/2023

Document Id: 0724426c-984b-1937-e063-6294a90a1cf5

Set id: cc9719ec-7e22-48bc-85cc-6835b6c31860

Version: 3

Effective Time: 20231007

Hampshire Laboratories Inc