NDC 40104-432 Modesa 2 In 1 Dandruff Almond Oil Dry Scalp
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 40104 - Ningbo Pulisi Daily Chemical Products Co., Ltd.
- 40104-432 - Modesa 2 In 1 Dandruff Almond Oil Dry Scalp
Product Packages
NDC Code 40104-432-01
Package Description: 396.9 g in 1 PACKAGE
Product Details
What is NDC 40104-432?
What are the uses for Modesa 2 In 1 Dandruff Almond Oil Dry Scalp?
Which are Modesa 2 In 1 Dandruff Almond Oil Dry Scalp UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
Which are Modesa 2 In 1 Dandruff Almond Oil Dry Scalp 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)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- ZINC SULFATE (UNII: 89DS0H96TB)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CITRIC ACID, 1-STEARYL ESTER (UNII: E945AJ51FA)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Modesa 2 In 1 Dandruff Almond Oil Dry Scalp?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
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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".