NDC 70477-103 Therapytion Natural Relaxing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70477 - 360 Perspective
- 70477-103 - Therapytion Natural Relaxing
Product Packages
NDC Code 70477-103-02
Package Description: 1 BOTTLE in 1 PACKAGE / 500 mL in 1 BOTTLE (70477-103-01)
Product Details
What is NDC 70477-103?
Which are Therapytion Natural Relaxing UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Therapytion Natural Relaxing 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CARROT (UNII: L56Z1JK48B)
- BEACH STRAWBERRY (UNII: 98542F2TQS)
- ROSEMARY (UNII: IJ67X351P9)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- SALVIA OFFICINALIS ROOT (UNII: 236QY0A1BL)
- LUFFA AEGYPTIACA FRUIT (UNII: QKL9NEO1F9)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
- HEDERA HELIX LEAF (UNII: ZP9XFG71A7)
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- GRAPEFRUIT (UNII: O82C39RR8C)
- PERILLA FRUTESCENS TOP (UNII: T4L5881Y68)
- ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX)
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[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".