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Dream cream - Medication Information

Product NDC Code 70722-232
Drug Name

Dream cream

Type Brand
Active Ingredients
Camphor (natural) .45 g/100g
Menthol, unspecified form 5 g/100g
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 1812330
Application Number part348
Labeler Name Little Moon Essentials
Packages
Package NDC Code Description
70722-232-02 56.7 g in 1 container (70722-232-02)
70722-232-04 113 g in 1 container (70722-232-04)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Drug Facts Active Ingredients Camphor 0.45% Menthol 5%

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.
Purpose Topical Analgesic

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water (aqua) organic safflower oil (cathamus tictorius) beeswax (cera alba) cetearyl olivate arnica oil (arnica montana) castor oil (ricinus communis) cetearyl alcohol wintergreen oil (gaultheria procumbens) xanthan gum cinnamon oil (cinnamomum zeylanicum) lavender oil (lavendula angustifolia) cyprus oil (cupressus sempervirens) eucalytus blue mallee oil marjorm (thymus mastichina) rosemary oil (rosmarinus officinalis) juniper oil (juniperus communis) magnesium aluminum silicate immortelle oil (helichrysum angustifolium) clary sage oil (salvia sclarea) tea tree oil (melaleuca alternifolia) peppermint oil (mentha piperita) basil oil (ocimum basilicum) ginger (zingiber officinale) benzoin (styrax benzoin resin extract) potassium sorbate sodium benzoate

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.
Directions Adults and chidren over 12 years: Apply a thin layer to affected area Massage into painful area until thoroughly absorbed into skin repeat as necessary, but no moore than 3to 4 times daily, allowing minimum of 2-3 hours between applications AFTER APPLYING, WASH HANDS WITH SOAP AND WATER Children 12 years or younger: ask a doctor

Purpose

Information about the drug product’s indications for use.
Uses Uses temporarily relieves minor pain associated with simple backache muscle strains sprains bruises

Spl product data elements

Usually a list of ingredients in a drug product.
Dream Cream Camphor, Menthol MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM WATER CAMPHOR (NATURAL) CAMPHOR (NATURAL) CETOSTEARYL ALCOHOL SAFFLOWER OIL YELLOW WAX CETEARYL OLIVATE ARNICA MONTANA CASTOR OIL METHYL SALICYLATE XANTHAN GUM CINNAMON OIL SWEET MARJORAM GINGER POTASSIUM SORBATE SODIUM BENZOATE LAVENDER OIL CUPRESSUS SEMPERVIRENS LEAF OIL EUCALYPTUS POLYBRACTEA LEAF OIL ROSEMARY OIL JUNIPER BERRY OIL MAGNESIUM ALUMINUM SILICATE PSEUDOGNAPHALIUM LUTEOALBUM WHOLE CLARY SAGE OIL TEA TREE OIL PEPPERMINT OIL BASIL OIL BENZOIN RESIN

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.
Principle Display Panel 56.7 g container 2oz Dream Cream

Instructions for use

Information about safe handling and use of the drug product.
Other information Store at 68-77º​F (20-25ºC) Protect from excessive moisture

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 Condition worsens Redness is present Irritation develops Symptoms persist for more than 7 days or clear up and occur again within afew days You experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast feeding Ask a health professional before use.

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.
Warning For external use only When using this product Use only as directed Read and follow all directions and warnings on this label Rare cases of serious burns have been reported with products of this type Do not bandage tightly or apply local heat (such as heating pads)or medicated patches to the area of use Avoid contact with eyes and mucous membranes Do not apply to wounds or damages, broken or irritated skin A trasient burning sensation may occur upon application but generally dissapears in several days

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