Label: DR. PHILLIPS FORMULATIONS MUSCLE JOINT RELIEF- menthol, methyl salicylate, camphor bark oil, eucalyptus leaf oil cream
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Contains inactivated NDC Code(s)
NDC Code(s): 73183-100-11 - Packager: Dr. Phillips Formulations, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated December 29, 2020
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- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- DOSAGE & ADMINISTRATION
- WARNINGS
- INDICATIONS & USAGE
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INACTIVE INGREDIENT
Aqua, Butyrospermum Parkii (Shea) Butter, Cetearyl Glucoside, Cetearyl Alcohol, Cinnamomum Camphora, Glyceryl Stearate Citrate, CBD Hemp Extract, Prganic Aloe Barbadensis (Aloe Vera) leaf Juice, Tapioca Starch Modified, CLycerin, Caprylic, Capric Triglyceride, Xanthan Gum, Organic Rosmariun Officianalis (Rosemary) Leaf Extract, Organic Arnica Extract, Glyceryl Caprylate, Caprylhydroxamic Acid, Citric Acid
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. PHILLIPS FORMULATIONS MUSCLE JOINT RELIEF
menthol, methyl salicylate, camphor bark oil, eucalyptus leaf oil creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73183-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 10 mg in 100 mg METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 10 mg in 100 mg EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL 2 mg in 100 mg CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 3 mg in 100 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) XANTHAN GUM (UNII: TTV12P4NEE) SHEA BUTTER (UNII: K49155WL9Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73183-100-11 95500 mg in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/29/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 07/29/2019 Labeler - Dr. Phillips Formulations, LLC (117077993) Establishment Name Address ID/FEI Business Operations Royal Labs Natural Cosmetic, Inc. 197478480 manufacture(73183-100)