Label: TERRAFREEZE PAIN RELIEF- menthol,methyl salicylate,histamine dihydrochloride cream
- NDC Code(s): 71805-855-00
- Packager: Beyond Derma, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses:
-
Warnings:
- For External use only
- Keep out of reach of children. If swallowed, consult physician.
- Do not apply to wounds or damaged skin.
When using this product
- Avoid contact with eyes. If product gets into eyes, rinse thoroughly with water
- Do not bandage tightly
- Directions
- Other Information
-
Other Ingredients
Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Extract, AScorbic Acid (Vitamin C), Bosewellia Serrata Extract, Bromelain, Butylene Glycol, C13-14 Isoparaffin, Chamomilla Recutta (Chamomile) Extract, Citric Acid, Curcuma Longa (Turmeric) Extract, Emu Oil, Ethylhexylglycerin, Ethylhexyl Stearate, Glycyrrhiza Glabra (licorice) Root Extract, Helianthus Annuus (Sunflower) Oil, Laureth-7, magnesium Sulfate, Methylsulfonylmethane (MSM), Niacin, Phenoxyethanol, Polyacrylamide, Polysorbate-80, Potassium Sorbate, Sodium Polyacrylate, Tetrasodium EDTA, Tocopheryl Acetate (Vitamin E), Tricedeth-6, Zingiber Officinale (Ginger) Root Extract
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INGREDIENTS AND APPEARANCE
TERRAFREEZE PAIN RELIEF
menthol,methyl salicylate,histamine dihydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71805-855 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 100 mg in 1 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 100 mg in 1 g HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE 0.5 mg in 1 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARNICA MONTANA (UNII: O80TY208ZW) ASCORBIC ACID (UNII: PQ6CK8PD0R) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) BROMELAINS (UNII: U182GP2CF3) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) TURMERIC (UNII: 856YO1Z64F) EMU OIL (UNII: 344821WD61) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) LICORICE (UNII: 61ZBX54883) SUNFLOWER OIL (UNII: 3W1JG795YI) LAURETH-7 (UNII: Z95S6G8201) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) NIACIN (UNII: 2679MF687A) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) EDETATE SODIUM (UNII: MP1J8420LU) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIDECETH-6 (UNII: 3T5PCR2H0C) GINGER (UNII: C5529G5JPQ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71805-855-00 1 in 1 BOX 10/12/2017 1 57 g in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 10/12/2017 Labeler - Beyond Derma, LLC (080699834)