NDC 40104-434 Modesa Dandruff Everyday Clean

NDC Product Code 40104-434

NDC CODE: 40104-434

Proprietary Name: Modesa Dandruff Everyday Clean What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 40104 - Ningbo Pulisi Daily Chemical Products Co., Ltd.

NDC 40104-434-01

Package Description: 396.9 g in 1 PACKAGE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Modesa Dandruff Everyday Clean with NDC 40104-434 is a product labeled by Ningbo Pulisi Daily Chemical Products Co., Ltd.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 209884.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • 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)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Ningbo Pulisi Daily Chemical Products Co., Ltd.
Labeler Code: 40104
Start Marketing Date: 04-02-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Modesa Dandruff Everyday Clean Product Label Images

Modesa Dandruff Everyday Clean Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active Ingredient                                               PurposePyrithione Zinc             1.00%                            Anti-dandruff

Otc - Purpose

Help prevent to treat flakes, itch, irritation, oilness or dryness caused by dandruff.

Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222)right away.Avoid contact with eyes, if contact occurs rinse eyes with plenty of water.

Indications & Usage

Shake well.for maximum dandruff control, use every time you shampoo.wet hair, squeeze small amount to palm, lather, rinse well for best results use at least twice a week or as directed by a doctor.

Warnings

For external use only.Stop use and ask a doctor if Condition worsens or does not improve after regular use as directed.

Dosage & Administration

Small amount to palm, or as directed by a doctor.

Inactive Ingredient

Water, sodium laureth sulfate, sodium lauryl sulfate, cocamide MEA, zinc barbonate, glycol distearate, amodimethicone, fragrance, cetyl alcohol, sodium chloride, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, ammonium laureth sulfate, benzyl alcohol, sodium chloride, Trideceth-12, cetrimonium chloride, sodium xylenesulfonate, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 4.

* Please review the disclaimer below.