NDC 81702-202 Dr. Pelo Scalp-shampoo
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81702 - Jrj.,inc
- 81702-202 - Dr. Pelo Scalp-shampoo
Product Packages
NDC Code 81702-202-01
Package Description: 300 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 81702-202?
What are the uses for Dr. Pelo Scalp-shampoo?
Which are Dr. Pelo Scalp-shampoo UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Dr. Pelo Scalp-shampoo 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)
- HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)
- ROSEMARY (UNII: IJ67X351P9)
- REYNOUTRIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)
- MORUS ALBA BARK (UNII: 7O71A48NDP)
- COIX LACRYMA-JOBI VAR. MA-YUEN SEED (UNII: 8DW238I7ZI)
- HYALURONIC ACID (UNII: S270N0TRQY)
- ROSA CANINA FLOWER OIL (UNII: DUY7M48I1T)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- NIACINAMIDE (UNII: 25X51I8RD4)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- BIOTIN (UNII: 6SO6U10H04)
- WATER (UNII: 059QF0KO0R)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
* 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".