Amplify Relief Mm
Product Images NDC 69837-019

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Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Amplify Relief Mm (NDC 69837-019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by International Brand Management, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Image Description (Amplify V1)

Image Description (Amplify V1)
AMPIify Relief MM is a topical pain relief cream that contains Menthol 10% / Methyl Salicylate 30%. It is intended for temporary relief of minor aches and pains associated with strains, sprains, bruises, and simple backache. It is for external use only, and should not be used on wounds or damaged skin, with a heating pad, or with fabrics or clothing. It should not be used by children under 12 years of age without consulting a doctor. If symptoms persist for more than seven days or worsen, or if irritation occurs, one should consult a medical professional. The cream comes in a 4 oz tube.*
FDA Label Image

Image Description (Label)

Image Description (Label)
WPR Plus is a hydrogel wound dressing containing Lidocaine HCI USP 4%, indicated for painful wounds like post-surgical incisions, cuts and abrasions. It comes in a 30ml Amplify Relief MM 118ยข bottle and is applied to the affected area as directed, with a maximum of 12 pumps per day. LDO Plus should be used with caution in elderly, debilitated patients, children, and patients with known hypersensitivity of local anesthetics of the amide type. The drug is contraindicated in patients with hypersensitivity to local anesthetics of the amide type or other components of LDO Plus. Side effects include redness or swelling at the application site, and in rare cases, symptoms like sluggishness, confusion, slow breathing, low blood pressure, or slow heartbeat may occur. Adverse reactions can be caused by excessive dosage or hypersensitivity, idiosyncrasy or diminished tolerance on the part of the patient.*
FDA Label Image

Image Description (Label2)

Image Description (Label2)
This text provides information on drug interactions, use in specific populations, onset of anesthesia, hemodynamics, pharmacokinetics, non-clinical toxicity, and storage of LDO Plus, a medicated hydrogel containing Lidocaine Hydrochloride USP for topical administration. It is cautioned to use with precaution in patients receiving antiarrhythmic drugs and is not recommended for children under 2 without physician direction. It is also advised to store and dispose of this and all medications out of reach of children and pets.*
FDA Label Image

Label3 (Label3)

Label3 (Label3)
AMPLIFY RELIEF MM is a topical analgesic cream containing 30.00% Methyl Salicylate and 10.00% Menthol as active ingredients, designed to temporarily relieve minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains. The cream is not intended for use on wounds or damaged skin or with a heating pad, and use on a child under 12 years of age with arthritis-like conditions should not occur without consulting with a doctor. Other ingredients include hemp seed oil, aloe vera gel, and glucosamine sulfate. Keep AMPLIFY RELIEF MM out of reach of children to avoid accidental ingestion, and if symptoms persist for more than 7 days, a doctor should be consulted. AMPLIFY RELIEF MM is distributed by the Drug Place Inc. and should be used as directed.*
FDA Label Image

Label4 (Label4)

Label4 (Label4)
This is a product with the NDC (National Drug Code) number 69837-305-03. The product contains a Wound Healing System and Lidocaine HCI USP 4% with AMPIify Relief MM (Menthol 10.00% / Methyl Salicylate 30.00%)-118g. The enclosed insert contains full prescribing information. It is a soothing hydrogel wound dressing that promotes moist wound healing for the healing process. There are instructions on cleansing the wound and applying the product. However, the text appears to be gibberish, making it difficult to read and understand the full description.*
FDA Label Image

Structure (Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.