- ACTIVE INGREDIENTS
- PURPOSE
- USE:
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- PREGNANCY OR BREAST FEEDING
- DIRECTIONS
-
INACTIVE INGREDIENTS
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis (Aloe) Leaf Juice, Benzoic Acid, Boswellia Serrata Gum, Cetearyl Alcohol, Ethylhexylglycerin, Gaultheria Procumbens (Wintergreen) Leaf Extract, Glycereth-2 Cocoate, Glyceryl Stearate, Hydroxypropyl Methyl Cellulose, Isopropyl Palmitate, Peg-100 Stearate, Petasites Vulgaris( Butterbur) Leaf Extract, Phenoxyethanol, Pinus Pinaster Bark Bud Extract, Polysorbate 60, Propylene Glycol, Salix Alba (Willow) Bark Extract, Stearyl Alcohol, Water, Zanthoxylum Americanum( Prickly Ash) Bark Extract, Zingiber Officinale (Ginger) Root Extract
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ULTRACIN T
trolamine salicylate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55628-9047 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TROLAMINE SALICYLATE (UNII: H8O4040BHD) (SALICYLIC ACID - UNII:O414PZ4LPZ) TROLAMINE SALICYLATE 10 g in 100 mL Inactive Ingredients Ingredient Name Strength (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8) ALOE VERA LEAF (UNII: ZY81Z83H0X) BENZOIC ACID (UNII: 8SKN0B0MIM) BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GAULTHERIA PROCUMBENS LEAF (UNII: 2125M16OWN) GLYCERETH-2 COCOATE (UNII: JWM00VS7HC) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HYPROMELLOSES (UNII: 3NXW29V3WO) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) PEG-100 STEARATE (UNII: YD01N1999R) PETASITES HYBRIDUS LEAF (UNII: JOS311ZC1G) PHENOXYETHANOL (UNII: HIE492ZZ3T) MARITIME PINE (UNII: 50JZ5Z98QY) POLYSORBATE 60 (UNII: CAL22UVI4M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WILLOW BARK (UNII: S883J9JDYX) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) WATER (UNII: 059QF0KO0R) ZANTHOXYLUM AMERICANUM BARK (UNII: A4KL1HMZ7T) ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55628-9047-4 120 mL in 1 TUBE; Type 0: Not a Combination Product 08/04/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 08/04/2015 Labeler - Cal Pharma (078721283) Registrant - Cal Pharma (078721283)