- OxyRub Pain Relief Cream
- Active Ingredient
- Purpose
- Uses
-
Warnings
For external use only.
- Use only as directed.
Do not use
- with a heating pad, may blister skin
- on open wounds or damaged skin
Ask a doctor before use if you have redness over the affected area
When using this product- Avoid contact with eyes
- Do not bandage tightly
Stop use and consult a doctor if
- skin redness or excessive skin irritation develops
- condition worsens or symptoms persist for more than 7 days
- symptoms clear up and occur again in a few days
- Keep out of reach of children
- Directions
- Other information
- Inactive Ingredients
- OxyRub Pain Relief Cream 4oz/114g (65121-113-04)
-
INGREDIENTS AND APPEARANCE
OXYRUB PAIN RELIEF
menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65121-113 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1.25 g in 100 g Inactive Ingredients Ingredient Name Strength BITTER ORANGE OIL (UNII: 9TLV70SV6I) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) CAPRYLYL GLYCOL (UNII: 00YIU5438U) EUCALYPTUS OIL (UNII: 2R04ONI662) GLYCERIN (UNII: PDC6A3C0OX) LAURETH-7 (UNII: Z95S6G8201) CORN OIL (UNII: 8470G57WFM) POLYSORBATE 20 (UNII: 7T1F30V5YH) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65121-113-04 114 g in 1 TUBE; Type 0: Not a Combination Product 05/01/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 05/01/2013 Labeler - Pure Source, LLC (080354456) Registrant - Pure Source, LLC (080354456) Establishment Name Address ID/FEI Business Operations Pure Source, LLC 080354456 manufacture(65121-113)