Label: TRIDERMA LIPSORE CREAM- calendula officinalis cream
- NDC Code(s): 10738-020-55
- Packager: Genuine Virgin Aloe Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated February 7, 2023
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- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
•Read all package directions and warnings before use. When using this product use only as directed. Apply a thin layer to affected area and massage gently as soon as possible after minor injury. Apply 3X a day or as needed •Sensitivity Test for a New User. Apply sparingly to one or two small affected areas during the first 3 days. •if no discomfort occurs, follow the direction stated above.
- Other information
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Inactive ingredients
water, cetearyl alcohol, isopropyl palmitate, polysorbate 60, cera alba(beeswax), dimethicone, allantoin, zinc PCA, avena sativa (oat) kernel flour, aloe barbadensis leaf juice, butyrospermum parkii (shea) butter, tocopheryl acetate (vitamin E), panthenol (pro-vitamin B5), cetyl alcohol, sodium PCA, sodium phytate, sodium hydroxide, phenoxyethanol, ethylhexylglycerin.
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INGREDIENTS AND APPEARANCE
TRIDERMA LIPSORE CREAM
calendula officinalis creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10738-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP 1.5 g in 100 g Inactive Ingredients Ingredient Name Strength PHYTATE SODIUM (UNII: 88496G1ERL) SODIUM HYDROXIDE (UNII: 55X04QC32I) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WATER (UNII: 059QF0KO0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) POLYSORBATE 60 (UNII: CAL22UVI4M) YELLOW WAX (UNII: 2ZA36H0S2V) DIMETHICONE (UNII: 92RU3N3Y1O) ALLANTOIN (UNII: 344S277G0Z) ZINC PIDOLATE (UNII: C32PQ86DH4) OATMEAL (UNII: 8PI54V663Y) ALOE VERA LEAF (UNII: ZY81Z83H0X) SHEA BUTTER (UNII: K49155WL9Y) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PANTHENOL (UNII: WV9CM0O67Z) CETYL ALCOHOL (UNII: 936JST6JCN) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10738-020-55 14 g in 1 TUBE; Type 0: Not a Combination Product 04/27/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/27/2021 Labeler - Genuine Virgin Aloe Corporation (961374147) Establishment Name Address ID/FEI Business Operations Genuine Virgin Aloe Corporation 961374147 manufacture(10738-020)