Label: DOCTOR HOYS PAIN RELIEF GEL (menthol, camphor- synthetic gel
- NDC Code(s): 75638-010-00, 75638-010-01, 75638-010-02, 75638-010-03
- Packager: Dynamic Blending Specialists, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 21, 2023
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- Drug Facts:
- Active ingredients:
- Uses:
- Warnings:
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Directions:
For adults and children 2 years and older: For best results, shake well and apply generously. Use 1 layer for minor pain, 2 layers for medium and 3 layers for severe symptoms • Rub in well and allow to dry between layers (usually 2-3 minutes) • Repeat process up to 4 times daily • for children under 2 years of age: Consult a physician before use.
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Inactive ingedients:
Alcohol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Arnica Montana (Arnica Flower) Extract, Biosaccharide Gum-1, Butyrospermum Parkii (Shea) Butter Extract, Ethylhexylglycerin, Euphorbia Cerifera (Candelilla) Wax, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Hydrated Silica, Jojoba Esters, Phenoxyethanol, Polyglyceryl-10 Caprylate/Caprate, SD Alcohol 40-B, Sodium Starch Octenylsuccinate, Tocopherol Acetate, Water, Zanthoxylum Bungeanum Fruit Extract.
- 75638-010-00
- 75638-010-01
- 75638-010-02
- 75638-010-03
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INGREDIENTS AND APPEARANCE
DOCTOR HOYS PAIN RELIEF GEL
menthol, camphor (synthetic) gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75638-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 50 mg in 1 mL CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ARNICA MONTANA WHOLE (UNII: O80TY208ZW) BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H) SHEA BUTTER (UNII: K49155WL9Y) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CANDELILLA WAX (UNII: WL0328HX19) GLYCERIN (UNII: PDC6A3C0OX) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) HYDRATED SILICA (UNII: Y6O7T4G8P9) PHENOXYETHANOL (UNII: HIE492ZZ3T) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) ZANTHOXYLUM BUNGEANUM FRUIT (UNII: 3CIP16A418) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75638-010-00 89 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2023 2 NDC:75638-010-01 177 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2023 3 NDC:75638-010-02 946 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2023 4 NDC:75638-010-03 1893 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 03/01/2023 Labeler - Dynamic Blending Specialists, Inc. (085704438)