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Product NDC Code | 76348-480 | ||||
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Drug Name | Natural relief 1222 |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | LOTION | ||||
Labeler Name | RENU LABORATORIES, INC. | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Bryonia 6x HPUS 1% Rhus Toxicodendron 6x HPUS 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 Apply a small amount of Natural Relief 1222 to affected areas and massage into skin. Use first thing in the morning, before bed, and whenever aches and stiffness flare up.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Water, Cetearyl Alcohol, Ceteareth-20, Squalene, Propylene Glycol, Prunus Amygdalus Dulcis Oil, Glycine Soja Oil, Stearic Acid, Tocopherol, Aloe Barbadensis Leaf Juice, SD Alcohol 40-B, Myristyl Myristate, Hydrolyzed Elastin, Hydrolyzed Keratin, Allium Sativum Bulb Extract, Fragrance, Triethanolamine, Menthol USP, Phenoxyethanol, Benzoic Acid, Dehydroacetic Acid
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.Temporry relief of minor pain and stiffness of muscles and joints.
Purpose
Information about the drug product’s indications for use.Muscle aches and stiffness Joint pain and muscle stiffness
Spl product data elements
Usually a list of ingredients in a drug product.Natural Relief 1222 Bryonia 6x, Rhus Toxicodendron 6x STEARIC ACID PHENOXYETHANOL GARLIC TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF PROPYLENE GLYCOL MYRISTYL MYRISTATE BRYONIA ALBA ROOT BRYONIA ALBA ROOT SQUALANE WHITE WAX WATER TROLAMINE .ALPHA.-TOCOPHEROL HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW) MARINE COLLAGEN, SOLUBLE MENTHOL ALMOND OIL SOYBEAN OIL ALOE VERA LEAF BENZOIC ACID DEHYDROACETIC 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.Natural Relief 1222 Label NATURAL RELIEF 1222 LABEL FOR 32 OZ. 32 oz. NR1222
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.
Other safety information
Information about safe use and handling of the product that may not have been specified in another field.Store at 68 ° to 77° F.
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 persists for more than 3 days or worsens.
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.For external use only Avoid contact with eyes and open wounds. Stop use and ask a doctor if condition persists for more than 3 days or worsens. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use this product if you are hypersensitive to any of the ingredients. Stop use and ask a doctor if condition persists for more than 3 days or worsens. Keep out of reach of children.
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