Label: BODY DERM- calendula officinalis gel
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Contains inactivated NDC Code(s)
NDC Code(s): 73405-101-01 - Packager: Welife Technology Corp
- Category: HUMAN OTC DRUG LABEL
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 November 22, 2019
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- Drug Facts
- Active Ingredients
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INACTIVE INGREDIENTS
Purified Water, Glycerin, Lubragel NP (Glyceryl Acrylate/Acrylic Acid Copolymer), MSM( Methylsulfonylmethane), Xylitylglucoside-Anydroxylitol-Xylitol, Potassium Azeloyl Diglycinate, Vitamin E, Rye Serum, Hedychium Coronarium Root Extract, Phenoxyethanol, Carbopol Ultrez 10, Beta Glucam, Nettle Leaf, White Willow, Linden, Yucca Root, Aloe Vera Barbadensis Leaf Extract, Cucumis Sativus (Cucumber) Fruit Extract, Hyaluronic Acid, Resveratrol, Ginkgo Biloba Leaf Extract, Cucumber Fragrance, Sodium Bicarbonate, Somatropin (HGH) 30X.
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INGREDIENTS AND APPEARANCE
BODY DERM
calendula officinalis gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73405-101 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 [hp_X] in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) XYLITYLGLUCOSIDE (UNII: O0IEZ166FB) ANHYDROXYLITOL (UNII: 8XWR7NN42F) XYLITOL (UNII: VCQ006KQ1E) POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) HEDYCHIUM CORONARIUM ROOT (UNII: 92A6N0IQN9) PHENOXYETHANOL (UNII: HIE492ZZ3T) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) TRANSFORMING GROWTH FACTOR BETA RECEPTOR TYPE 3 (UNII: 18YWT2KYS8) URTICA DIOICA SUBSP. DIOICA LEAF (UNII: 232L6DS3Y4) SALIX ALBA WHOLE (UNII: V8UV0R324S) LINDEN LEAF (UNII: RU6O456OJ1) YUCCA SCHIDIGERA ROOT (UNII: E2H9ET15AT) ALOE VERA LEAF (UNII: ZY81Z83H0X) CUCUMBER (UNII: YY7C30VXJT) HYALURONIC ACID (UNII: S270N0TRQY) RESVERATROL (UNII: Q369O8926L) GINKGO (UNII: 19FUJ2C58T) SODIUM BICARBONATE (UNII: 8MDF5V39QO) SOMATROPIN (UNII: NQX9KB6PCL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73405-101-01 100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/21/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/21/2019 Labeler - Welife Technology Corp (111367674)