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Product NDC Code | 62001-0330 | ||||
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Drug Name | The original mane n tail daily control 2 in 1 anti dandruff |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | SHAMPOO | ||||
Application Number | M | ||||
Labeler Name | Straight Arrow Products Inc | ||||
Packages |
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Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient Pyrithione Zinc 1%
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.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 ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients: Water/Aqua/Eau(Water), Sodium Laureth Sulfate, Cocamide MEA, Sodium Lauryl Sulfate, Acrylates Copolymer, Coco Glucoside, Cocamidopropyl Betaine, PPG-2 Hydroxyethyl Coco/Isostearamide, Dimethicone, Polyquaternium-10, Theobroma Cocao (cocoa) Seed Butter, Polyquaternium-47, Laureth-4, Laureth-7, Sodium Chloride, Fragrance (Parfum), Citric Acid, Sodium Hydroxide, Caprylic/Capric Triglyceride, Prunus Amagdalus Dulcis (Sweet Almond) Seed Oil, Olea Europaea (Olive) Fruit Oil, Olea Europaea (Olive) Leaf Extract, Equisetum Arvense (Horsetail) Leaf Extract, Larrea Divaricata (Chaparral) Extract, Tussilago Farfara (Coltsfoot) Flower Extract, Aesculus Hippocastanum (Horse Chestnut) Seed Extract, Spiraea Ulmaria (Meadowsweet) Flower Extract, Trifolium Pratense (Clover) Flower Extract, Methylchloroisothiazolinone, Methylisothiazolinone, Benzyl Benzoate, Coumarin, Hydroxycitronellal, Butylphenyl Methylpropional, Alpha-isomethyl ionone, Limonene, Linalool, Blue 1 (CI 42090), Yellow 5 (CI 19140).
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Use - helps prevent recurrence of flaking and itchng associated with dandruff.
Purpose
Information about the drug product’s indications for use.Purpose Anti-dandruff
Spl product data elements
Usually a list of ingredients in a drug product.The Original Mane n Tail Daily Control 2 in 1 Anti Dandruff PYRITHIONE ZINC PYRITHIONE ZINC PYRITHIONE ZINC WATER SODIUM LAURETH SULFATE COCO MONOETHANOLAMIDE SODIUM LAURYL SULFATE BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) COCO GLUCOSIDE COCAMIDOPROPYL BETAINE PPG-2 HYDROXYETHYL COCO/ISOSTEARAMIDE DIMETHICONE POLYQUATERNIUM-10 (400 CPS AT 2%) COCOA BUTTER POLYQUATERNIUM-47 (METHACRYLAMIDOPROPYLTRIMETHYLAMMONIUM CHLORIDE-CO-METHYL ACRYLATE-CO-ACRYLIC ACID 45:10:45; 1200000 MW) LAURETH-4 LAURETH-7 SODIUM CHLORIDE ANHYDROUS CITRIC ACID SODIUM HYDROXIDE MEDIUM-CHAIN TRIGLYCERIDES ALMOND OIL OLIVE OIL OLEA EUROPAEA LEAF EQUISETUM ARVENSE BRANCH LARREA DIVARICATA LEAF TUSSILAGO FARFARA FLOWER HORSE CHESTNUT FILIPENDULA ULMARIA FLOWER TRIFOLIUM PRATENSE FLOWER METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE BENZYL BENZOATE COUMARIN HYDROXYCITRONELLAL BUTYLPHENYL METHYLPROPIONAL ISOMETHYL-.ALPHA.-IONONE LIMONENE, (+)- LINALOOL, (+/-)- FD&C BLUE NO. 1 FD&C YELLOW NO. 5
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.The Original Mane n Tail Daily Control 2 in 1 Anti Dandruff The Original Mane n Tail Daily Control 2 in 1 Anti Dandruff Front The Original Mane n Tail Daily Control 2 in 1 Anti Dandruff Back
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use and ask a doctor if condition worsens or does not improve after regular use as directed.
When using
Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.when using this product • do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings - For external use only when using this product • do not get into 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 as directed. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API