NDC 61310-101 Morreturn Hair Care
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61310 - Moreand Co., Ltd.
- 61310-101 - Morreturn Hair Care
Product Packages
NDC Code 61310-101-02
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 500 mL in 1 BOTTLE, PUMP (61310-101-01)
Product Details
What is NDC 61310-101?
Which are Morreturn Hair Care UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- BIOTIN (UNII: 6SO6U10H04)
- BIOTIN (UNII: 6SO6U10H04) (Active Moiety)
Which are Morreturn Hair Care Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ZANTHOXYLUM PIPERITUM FRUIT PULP (UNII: 7PFC2VA251)
- USNEA BARBATA (UNII: D6DVA9TCAP)
- PULSATILLA KOREANA WHOLE (UNII: 5R35881OBK)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- LAURETH-23 (UNII: N72LMW566G)
- C12-15 PARETH-3 (UNII: 459EF9MP3Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".