Dr. Freds MIRACLE RUB description, usages, side effects, indications, overdosage, supplying and lots more!

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Dr. Freds MIRACLE RUB

Pure Source Inc.

Dr. Fred's MIRACLE RUB


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Dr. Fred's MIRACLE RUB


Active Ingredients:

Histamine Dihydrochloride 0.025%

Purpose

External Analgesic

Uses:

For temporary relief of minor aches and pains associated with simple backache, arthritis, bruises and sprains.

Warnings:

- For external use only.
- Avoid contact with eyes.
- Do not apply to open wounds or damaged skin.

- If symptoms

persist for more than seven days, discontinue use and consult physician.

- Keep out of reach of children.

If swallowed, consult physician.

Do not use

if you have a known allergy to any of the ingredients listed.
- Do not bandage tightly.

- If pregnant or breast feeding,

contact physician prior to use.

Directions:

Apply directly to affected area. Do not use more than four times per day.

Other Ingredients:

Aloe Barbadensis Leaf (Aloe Vera Juice) Gel, Aqua (Deionized Water), Arnica Montana Extract, Carbomer, C13-14 Isoparaffin, Cetearyl Olivate, Dimethyl Sulfone (MSM), Laureth-7, Magnesium Sulfate, Parfum (Fragrance), Polyacrylamide, Potassium Sorbate, Royal Jelly, Sodium Benzoate, Sodium Stearate, Sorbitan Olivate, Stearic Acid, Triethanolamine.

Manufactured for:

Haleivo, Inc.
Ojai, Ca 93023 USA
www.DrFredsMeds.com

KNOCK OUT PAIN WITH
Dr. Fred's MIRACLE RUB  OJAI ORIGINAL
PATENT PENDING

4 FL. OZ. (118 ML)

Dr. Fred's MIRACLE RUB 4oz/118ml (65121-403-25)

Dr. Freds MIRACLE RUB

Dr. Freds MIRACLE RUB

HISTAMINE DIHYDROCHLORIDE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65121-403
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HISTAMINE DIHYDROCHLORIDE Histamine 0.25 mg

Inactive Ingredients

Ingredient Name Strength
Aloe Vera Leaf
water
ARNICA MONTANA
C13-14 ISOPARAFFIN
CETEARYL OLIVATE
DIMETHYL SULFONE
LAURETH-7
MAGNESIUM SULFATE
POTASSIUM SORBATE
ROYAL JELLY
SODIUM BENZOATE
sodium stearate
SORBITAN OLIVATE
STEARIC ACID
TROLAMINE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 118 in 1 BOTTLE
2 NDC:65121-403-25 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-06-06


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Be sure to consult your doctor before taking any medication!
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