NDC 51769-140 Head And Shoulders Hair Loss Prevention

NDC Product Code 51769-140

NDC 51769-140-01

Package Description: 10 mL in 1 POUCH

NDC 51769-140-05

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC 51769-140-11

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC 51769-140-18

Package Description: 1180 mL in 1 BOTTLE, PLASTIC

NDC 51769-140-20

Package Description: 200 mL in 1 BOTTLE, PLASTIC

NDC 51769-140-40

Package Description: 400 mL in 1 BOTTLE, PLASTIC

NDC 51769-140-50

Package Description: 500 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Head And Shoulders Hair Loss Prevention with NDC 51769-140 is a product labeled by All Natural Dynamics. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated to this product: 1043244 and 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)
  • SODIUM LAURYL SULFATE (UNII: 368GB5141J)
  • COCO MONOETHANOLAMIDE (UNII: C80684146D)
  • ZINC CARBONATE (UNII: EQR32Y7H0M)
  • GLYCOL DISTEARATE (UNII: 13W7MDN21W)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
  • MAGNESIUM SULFATE (UNII: DE08037SAB)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Labeler Information

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

Labeler Name: All Natural Dynamics
Labeler Code: 51769
Start Marketing Date: 02-01-2013 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: 12-31-2017 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.

Information for Patients

Selenium Sulfide

Selenium Sulfide is pronounced as (se lee' nee um)

Why is selenium sulfide medication prescribed?
Selenium sulfide, an anti-infective agent, relieves itching and flaking of the scalp and removes the dry, scaly particles that are commonly referred to as dandruff or seb...
[Read More]

* Please review the disclaimer below.

Head And Shoulders Hair Loss Prevention Product Label Images

Head And Shoulders Hair Loss Prevention 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

Other

Drug Facts

Dist. byProcter & Gamble Manufactura, S. de R.L. de C.V.San Andr`s Atoto No. 326, Naucalpan de Juarez,Estado de Mexico, MXwww.headandshoulders.com

Active Ingredient

Pyrithione zinc 1%

Purpose

Anti-dandruff

Uses

Helps prevent recurrence of flaking and itching associated with dandruff.helps prevent hair loss

Warnings

For external use only.

When Using This Product

  • Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor If

  • Condition worsens or does not improve after regular use of this product as directed.

Otc - Keep Out Of Reach Of Children

Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • For maximum dandruff control, use every time you shampoo.wet hair, massage onto scalp, rinse, repeat if desired.for best results use at least twice a week or as directed by a doctor.

Inactive Ingredients

Water, Sodium laureth sulfate, Sodium lauryl sulfate, Coco Monoethanolamide, Zinc carbonate, Glycol distearate, Dimethicone, Guar hydroxypropyltrimonium chloride, Magnesium sulfate, Sodium benzoate, Magnesium carbonate hydroxide, Benzyl alcohol, Tocopheryl acetate, FD&C Yellow No. 5, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Blue no. 1

* Please review the disclaimer below.