Label: ARTHRITIS PLUS GEL- camphor, menthol, methyl salicylate cream
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Contains inactivated NDC Code(s)
NDC Code(s): 50810-2000-1 - Packager: JI Well Health Company
- Category: HUMAN OTC DRUG LABEL
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 June 5, 2013
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- Official Label (Printer Friendly)
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INACTIVE INGREDIENT
Inactive Ingredients
Aloe vera gel, amica montana (flower extract), cetaryl alcohol, clove oil,
diazolidimyl urea, FD C Blue #1, frangrance, ginger oil, lavender oil,
methylsulfonylmethane (MSM), Methyl paraben, orange oil.
peppermint oil, polysorbate 60, propylene glycol, propylparaben,
purified water, rosemary oil, thyme oil, Vitamin C,
Vitamin E, xanthan gum
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings:
For external use only. Avoid contact with
eyes and mucous membranes
-If condition worsens or if symptoms persist for more than 7 days
or clear up and appear again within a few days, discontinue use of this
product and consult a doctor.
-When used for arthritis, if pain persists for more than 10 days or redness
is present or in conditions affecting children under 12 years of age, consult
a physician immediately.
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ARTHRITIS PLUS GEL
camphor, menthol, methyl salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50810-2000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 3 mg in 100 mg MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 12 mg in 100 mg METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 15 mg in 100 mg Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ARNICA MONTANA (UNII: O80TY208ZW) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CLOVE OIL (UNII: 578389D6D0) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) GINGER OIL (UNII: SAS9Z1SVUK) LAVENDER OIL (UNII: ZBP1YXW0H8) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) METHYLPARABEN (UNII: A2I8C7HI9T) ORANGE OIL (UNII: AKN3KSD11B) PEPPERMINT OIL (UNII: AV092KU4JH) POLYSORBATE 60 (UNII: CAL22UVI4M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) ROSEMARY OIL (UNII: 8LGU7VM393) THYME OIL (UNII: 2UK410MY6B) ASCORBIC ACID (UNII: PQ6CK8PD0R) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50810-2000-1 1 in 1 BOX 1 57 mg in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 07/01/2013 Labeler - JI Well Health Company (005624801)