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Product NDC Code | 82707-101 | ||||||||
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Drug Name | Max pain relief |
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Type | Brand | ||||||||
Active Ingredients |
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Route | TOPICAL | ||||||||
Dosage Form | CREAM | ||||||||
Application Number | part348 | ||||||||
Labeler Name | PROVEDA | ||||||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.ACTIVE INGREDIENTS CAMPHOR 3.10% MENTHOL 3.10%
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 ADULTS 21 YEARS OF AGE AND OLDER: APPLY TO AFFECTED AREA NOT MORE THAN 3 TO 4 TIMES DAILY.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.INACTIVE INGREDIENTS WATER, EUCALYPTUS GLOBULUS LEAF OIL, MENTHA PIPERITA (PEPPERMINT) OIL, GAULTHERIA PROCUMBENS (WINTERGREEN) LEAF OIL, POLYSORBATE 80, SORBITAN STEARATE, PEG-8, PROPYLENE GLYCOL, ETHOXYDIGLYCOL, CANNABIDIOL (BROAD SPECTRUM HEMP EXTRACT), CANNABIDIOL, MENTHA SPICATA FLOWER/LEAF/STEM OIL, THYMUS VULGARIS (THYME) FLOWER/LEAF OIL, CETYL ALCOHOL, FRAGRANCE, OCIMUM BASILICUM (BASIL) OIL, EUGENIA CARYOPHYLLUS (CLOVE) BUD OIL, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL, CAPSICUM FRUTESCENS RESIN, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER OIL, ZINGIBER OFFICINALIS (GINGER) ROOT OIL, TRACHYSPERMUM AMMI FLOWER OIL, COMMIPHORA MYRRHA OIL, CITRUS AURANTIUM DULCIS (ORANGE) PEEL OIL, CHOLESTEROL, GLYCERYL DISTEARATE NF, GLYCERYL STEARATE, PEG-100 STEARATE, VITEX NEGUNDO EXTRACT, COMMIPHORA WIGHTII RESIN EXTRACT, HORDEUM VULGARE SEED EXTRACT, LECITHIN, CARBOMER
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.USES FOR THE TEMPORARY RELIEF OF MINOR ACHES AND PAINS OF MUSCLES AND JOINTS ASSOCIATED WITH: SIMPLE BACKACHE ARTHRITIS SPRAINS
Purpose
Information about the drug product’s indications for use.PURPOSE EXTERNAL ANALGESIC
Spl product data elements
Usually a list of ingredients in a drug product.MAX PAIN RELIEF CAMPHOR, MENTHOL HEMP THYME OIL CAPSICUM FRUTESCENS WHOLE GLYCERYL DISTEARATE CETYL ALCOHOL GLYCERYL MONOSTEARATE PEG-100 STEARATE GINGER OIL MYRRH OIL VITEX NEGUNDO WHOLE HORDEUM VULGARE WHOLE PEPPERMINT OIL PROPYLENE GLYCOL CLOVE OIL ROSEMARY OIL CHAMOMILE FLOWER OIL GAULTHERIA PROCUMBENS WHOLE POLYSORBATE 80 POLYETHYLENE GLYCOL 400 COMMIPHORA WIGHTII RESIN CARBOMER 940 LECITHIN, SOYBEAN EUCALYPTUS OIL PEG-6 SORBITAN STEARATE DIETHYLENE GLYCOL MONOETHYL ETHER MENTHA SPICATA OIL BASIL OIL WATER CANNABIS SATIVA WHOLE LAVENDER OIL TRACHYSPERMUM AMMI FLOWER ORANGE PEEL CHOLESTEROL MENTHOL MENTHOL CAMPHOR OIL CAMPHOR OIL
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.01b UC_Max Pain Relief Cream_50mL
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 IMMEDIATELY.
Questions
A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.QUESTIONS? CALL 855-776-8332
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 THE EYES DO NOT APPLY TO WOUNDS OR DAMAGED SKIN DO NOT BANDAGE TIGHTLY DISCONTINUE USE OF THIS PRODUCY AND CONSULT A DOCTOR IF CONDITION WORSENS SYMPTOMS PERSIST FOR MORE THAN 7 DAYS SYMPTOMS CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS IF PREGNANT OR BREAST FEEDING CONSULT A DOCTOR BEFORE USE DO NOT USE IF TAKING ANTICOAGULANTS OR HAVE BLEEDING DISORDERS.
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