Label: ALFLEXIL ZERO PAIN- camphor, lidocaine hcl, menthol gel
- NDC Code(s): 49283-145-03
- Packager: CHEMCO CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 14, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- Use
- WARNINGS
-
WHEN USING
Use only as directed
Do not bandage tightly or use with a heating pad.
Avoid contact with eyes and mucous membranes.
Do not apply to wounds or damaged, broken or irritated skin.
A transient burning sensation or redness may occur upon application but generally disappears in several days.
Do not use in large quantities, particularly over raw surfaces or blistered areas.
If you experience an allergic reaction, discontinue use and consult a physician.Do not expose the area treated with product to heat or direct sunlight.
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- Directions
- OTHER SAFETY INFORMATION
-
INACTIVE INGREDIENT
Water (Aqua), Alcohol Denat, Arnica Montana Flower Extract, Ceteareth-20, Propylene Glycol, Triethanolamine, Carbomer, Glycerin, Methyl Salicylate, Sodium Chondroitin Sulfate, Disodium EDTA, Glucosamine Sulfate, Tocopheryl Acetate, Rosmarinus Officinalis (Rosemary) Extract, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Blue No.1 (CI 42090).
- QUESTIONS
- ALFLEXIL ZERO PAIN ROLL-ON
-
INGREDIENTS AND APPEARANCE
ALFLEXIL ZERO PAIN
camphor, lidocaine hcl, menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49283-145 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 g in 100 g CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 0.5 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1 g in 100 g Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) CARBOMER 940 (UNII: 4Q93RCW27E) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) METHYL SALICYLATE (UNII: LAV5U5022Y) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) ARNICA MONTANA FLOWER WATER (UNII: U7L2JP51PR) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TROLAMINE (UNII: 9O3K93S3TK) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Product Characteristics Color blue Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49283-145-03 90 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 10/18/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 10/18/2023 Labeler - CHEMCO CORPORATION (032495954)