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Product NDC Code | 12022-041 | ||||
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Drug Name | Doo gro braids twists locs dandruff control moisturizing |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | LIQUID | ||||
RxCUI drug identifier | 1048903 | ||||
Application Number | M032 | ||||
Labeler Name | J. Strickland and Co. | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient Salicylic Acid, 2% Purpose Antidandruff
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 Spray to apply to the affected areas 1-4 times daily, or as directed by a doctor.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients Water, Glycerin, PEG-12 Dimethicone, Propylene Glycol, Sodium Hydroxide, Hydrolyzed Collagen, Disodium EDTA, Diazolidinyl Urea, Methylparaben, Propylparaben, Benzyl Alcohol, Benzyl Benzoate, Eugenol, Hydroxycitronellal, Linalool, Fragrance.
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: Controls scalp itching and flaking due to dandruff
Purpose
Information about the drug product’s indications for use.Purpose Antidandruff
Spl product data elements
Usually a list of ingredients in a drug product.Doo Gro Braids Twists Locs Dandruff Control Moisturizing SALICYLIC ACID WATER GLYCERIN PEG-12 DIMETHICONE PROPYLENE GLYCOL SODIUM HYDROXIDE EDETATE DISODIUM DIAZOLIDINYL UREA METHYLPARABEN PROPYLPARABEN BENZYL ALCOHOL BENZYL BENZOATE EUGENOL HYDROXYCITRONELLAL LINALOOL, (+/-)- SALICYLIC ACID SALICYLIC ACID
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.Package Labeling: Label
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.Drug Facts
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 call a poison control center at once.
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 consult a doctor if condition worsens or does not improve after regular use of this product 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 avoid contact with 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 avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Stop use and consult a doctor if condition worsens or does not improve after regular use of this product as directed. Keep out of reach of children. If swallowed, get medical help or call a poison control center at once.
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