NDC 64942-1249 Clear Men Strong And Full Antidandruff

NDC Product Code 64942-1249

NDC CODE: 64942-1249

Proprietary Name: Clear Men Strong And Full Antidandruff 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

  • 64942 - Conopco Inc. D/b/a Unilever

NDC 64942-1249-1

Package Description: 381 mL in 1 CONTAINER

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

NDC Product Information

Clear Men Strong And Full Antidandruff with NDC 64942-1249 is a product labeled by Conopco Inc. D/b/a Unilever. 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)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • SODIUM LAUROYL ISETHIONATE (UNII: M590021Z02)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • TEA-DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
  • SUNFLOWER OIL (UNII: 3W1JG795YI)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • PPG-9 (UNII: I29VQH0G0B)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • SPEARMINT OIL (UNII: C3M81465G5)
  • GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • PALMITIC ACID (UNII: 2V16EO95H1)
  • ZINC SULFATE (UNII: 89DS0H96TB)
  • DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • SODIUM ISETHIONATE (UNII: 3R36J71C17)
  • POLOXAMER 407 (UNII: TUF2IVW3M2)
  • LAURETH-23 (UNII: N72LMW566G)
  • LAURETH-4 (UNII: 6HQ855798J)
  • .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
  • ALMOND OIL (UNII: 66YXD4DKO9)
  • POLYETHYLENE GLYCOL 400000 (UNII: 439X29GCJZ)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)
  • HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
  • SOYBEAN OIL (UNII: 241ATL177A)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • ASIAN GINSENG (UNII: CUQ3A77YXI)
  • TEA TREE OIL (UNII: VIF565UC2G)

Product Labeler Information

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

Labeler Name: Conopco Inc. D/b/a Unilever
Labeler Code: 64942
Start Marketing Date: 05-09-2012 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: 12-31-2018 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.

Clear Men Strong And Full Antidandruff 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 IngredientPyrithione Zinc (1.0%)

Otc - Purpose

PurposeAntidandruff

Indications & Usage

Uses: helps prevent and control recurrence of itching and flaking associated with dandruff

Warnings

WarningsFor external use only

Otc - When Using

When using this product: avoid contact with eyes.  If contact occurs, rinse eyes thoroughly with water.

Otc - Stop Use

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.

Dosage & Administration

Directions: Wet hair, massage into scalp, rinse.  Repeat if desired.  For best results use at least twice a week or as directed by a doctor.

Inactive Ingredient

Inactive IngredientsWater (Aqua)Sodium Laureth SulfateCocamidopropyl BetaineSodium ChlorideFragrance (Parfum)DimethiconolCarbomerDimethiconeSodium Lauroyl IsethionateHelianthus Annuus (Sunflower) Seed OilDMDM HydantoinGuar Hydroxypropyltrimonium ChlorideStearic AcidCitric AcidTallow Acid or Palmitic AcidZinc SulfateTEA-DodecylbenzenesulfonateSodium IsethionatePoloxamer 407Laureth-23Laureth-4Tocopheryl AcetatePrunus Amygdalus Dulcis (Sweet Almond) OilPPG-9PanthenolLysine HClHydrogenated Coconut OilGlycine Soja (Soybean) OilMethylisothiazolinonePEG-9MXanthan GumMethylchloroisothiazolinonePanax Ginseng Root ExtractMentha Viridis (Spearmint) Leaf OilMelaleuca Alternifolia (Tea Tree) Flower/Leaf/Stem ExtractTitanium Dioxide (CI 77891)

Otc - Questions

Questions, comments?: 1-800-372-6389

* Please review the disclaimer below.