- DRUG FACTS
- Uses
- Warnings:
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Caution: Discontinue use if excessive irritation of the skin develops. Avoid getting into eyes or mucous membranes. If condition worsens, or symptoms persist for more than 7 days or clear up and occur again within a few days, or redness is present, or in conditions affecting children under 12 years of age, discontinue use and consult a physician immediately.
- Directions
-
Inactive Ingredients:
AQUA, PARAFFINUM LIQUIDUM, STEARIC ACID, GLYCERYL MONOSTEARATE, CETYL ALCOHOL, DIMETHICONE, GLYCERETH-26, PROPYLENE GLYCOL, DIAZOLIDINYL UREA, METHYLPARABEN, PROPYLPARABEN, STEARYL ALCOHOL, TRIETHANOLAMINE, ACRYLAMIDE, SODIUM ACRYLATE, TRIDECETH-6, SODIUM HYALURONATE, SODIUM PCA, WHEAT AMINO ACIDS, PANTHENOL, SYMPHYTUM OFFICINALE EXTRACT, HYDROXYPROLINE.
- Manufactured by:
- FAST RELIEF REUMACETIN
-
INGREDIENTS AND APPEARANCE
FAST RELIEF REUMACETIN
menthol, methyl salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49283-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 12.5 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2.5 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) MINERAL OIL (UNII: T5L8T28FGP) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CETYL ALCOHOL (UNII: 936JST6JCN) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERETH-26 (UNII: NNE56F2N14) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) TROLAMINE (UNII: 9O3K93S3TK) ACRYLAMIDE (UNII: 20R035KLCI) SODIUM ACRYLATE (UNII: 7C98FKB43H) TRIDECETH-6 (UNII: 3T5PCR2H0C) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) AMINO ACIDS, WHEAT (UNII: 0370GZL32F) PANTHENOL (UNII: WV9CM0O67Z) COMFREY LEAF (UNII: DG4F8T839X) HYDROXYPROLINE (UNII: RMB44WO89X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49283-006-08 226 g in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 08/26/2013 Labeler - Chemco Corporation (032495954) Registrant - Chemco Corporation (032495954) Establishment Name Address ID/FEI Business Operations Chemco Corporation 032495954 manufacture(49283-006)