Label: SHINMO SAENGBALEUM TREATMENT- panthenol gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 69978-002-01, 69978-002-02 - Packager: ATEC&CO INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated July 20, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
-
INACTIVE INGREDIENT
Water, Cetrimonium Chloride, Dimethicone, Trideceth-10, Cetearyl alcohol, Cetrimonium Chloride, Cyclopentasiloxane, Cyclohexasiloxane, BEHENYL ALCOHOL, Myristyl Alcohol, Butylene Glycol, Distearyldimonium Chloride, Stearamidopropyl Dimethylamine, Polyquaternium-10, Angelica Gigas Root Extract, Artemisia Princeps Leaf Extract, Sophora Angustifolia Root Extract, Cimicifuga Dahurica Root Extract, Angelica Dahurica Root Extract, Acorus Gramineus Root/Stem Extract, Punica Granatum Bark Extract, Saposhnikovia Divaricata Root Extract, Scutellaria Baicalensis Root Extract, Atractyloides Chinensis Rhizome Extract, Biota Orientalis Leaf Extract, Ceteareth-20, Benzyl Alcohol, Citric Acid, Betaine, Glycine Max (Soybean) Seed Extract, Lecithin, Simmondsia Chinensis (Jojoba) Seed Oil, Cetearyl Alcohol, Polysorbate 60, Sesamum Indicum (Sesame) Seed Extract, Oryza Sativa (Rice) Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Polygonum Multiflorum Root Extract, Camellia Sinensis Leaf Extract, Red Ginseng Extract, Portulaca Oleracea Extract, Rheum Palmatum Root Extract, Silkworm Extract, Bletia Hyacinthina Bulb Extract, Carthamus Tinctorius (Safflower) Flower Extract, Hydrolyzed Keratin, Caramel, Panthenyl Ethyl Ether, Methylchloroisothiazolinone, Methylisothiazolinone, Fragrance
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SHINMO SAENGBALEUM TREATMENT
panthenol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69978-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 0.95 g in 958.50 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) TRIDECETH-10 (UNII: G624N6MSBA) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CYCLOMETHICONE 6 (UNII: XHK3U310BA) DOCOSANOL (UNII: 9G1OE216XY) MYRISTYL ALCOHOL (UNII: V42034O9PU) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X) STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR) POLYQUATERNIUM-10 (400 MPA.S AT 2%) (UNII: HB1401PQFS) ANGELICA GIGAS ROOT (UNII: 32766B2FHX) ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) ACTAEA DAHURICA ROOT (UNII: 1D114JZ36B) ANGELICA DAHURICA ROOT (UNII: 1V63N2S972) ACORUS GRAMINEUS ROOT (UNII: Z60N6Q6E19) PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O) PLATYCLADUS ORIENTALIS LEAF (UNII: 32E5V7G32B) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) BENZYL ALCOHOL (UNII: LKG8494WBH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) BETAINE (UNII: 3SCV180C9W) SOYBEAN (UNII: L7HT8F1ZOD) EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) JOJOBA OIL (UNII: 724GKU717M) POLYSORBATE 60 (UNII: CAL22UVI4M) SESAME SEED (UNII: 7Y1255HVXR) RICE GERM (UNII: 7N2B70SFEZ) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ASIAN GINSENG (UNII: CUQ3A77YXI) PURSLANE (UNII: M6S840WXG5) RHEUM PALMATUM ROOT (UNII: G025DAL7CE) BLETILLA STRIATA BULB (UNII: 00T5SH6SEJ) SAFFLOWER (UNII: 4VBL71TY4Y) CARAMEL (UNII: T9D99G2B1R) PANTHENYL ETHYL ETHER (UNII: F4WMF8NX3B) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69978-002-02 1 in 1 CARTON 07/20/2015 1 NDC:69978-002-01 958.50 g in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/20/2015 Labeler - ATEC&CO INC. (689515243) Registrant - ATEC&CO INC. (689515243) Establishment Name Address ID/FEI Business Operations ATEC&CO INC. 689515243 manufacture(69978-002)
