Label: ACTIVON ULTRA STRENGTH ARTHRITIS- menthol, unspecified form stick
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Contains inactivated NDC Code(s)
NDC Code(s): 51068-507-01 - Packager: Family First Pharmaceuticals, Inc.
- 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 February 21, 2017
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only.
Do not use
- otherwise than as directed
- if you are allergic to any ingredient in this product
- on a child under 12 years of age with arthritis-like conditions
- with a heating pad
When using this product
- avoid contact with eyes, wounds, mucous membranes, broken or irritated skin
- do not share this product with anyone
- do not bandage tightly
- Directions
- Other information
- Inactive Ingredients
- Questions ?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 57 g Canister Carton
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INGREDIENTS AND APPEARANCE
ACTIVON ULTRA STRENGTH ARTHRITIS
menthol, unspecified form stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51068-507 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Menthol, Unspecified Form (UNII: L7T10EIP3A) (Menthol, Unspecified Form - UNII:L7T10EIP3A) Menthol, Unspecified Form 0.05138 g in 1 g Inactive Ingredients Ingredient Name Strength diazolidinyl urea (UNII: H5RIZ3MPW4) alcohol (UNII: 3K9958V90M) iodopropynyl butylcarbamate (UNII: 603P14DHEB) menthyl lactate, (-)- (UNII: 2BF9E65L7I) propylene glycol (UNII: 6DC9Q167V3) sodium stearate (UNII: QU7E2XA9TG) steareth-21 (UNII: 53J3F32P58) Edetate Sodium (UNII: MP1J8420LU) trolamine (UNII: 9O3K93S3TK) water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51068-507-01 1 in 1 CARTON 02/15/2017 1 57 g in 1 CANISTER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part348 02/15/2017 Labeler - Family First Pharmaceuticals, Inc. (832435809) Establishment Name Address ID/FEI Business Operations RNA Pharma, LLC 079103999 MANUFACTURE(51068-507)