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Dr. Freds MIRACLE RUB

Medically reviewed by Drugs.com. Last updated on Oct 19, 2021.

Dosage form: cream
Ingredients: HISTAMINE DIHYDROCHLORIDE 0.25mg in 1mL
Labeler: Pure Source, LLC
NDC Code: 65121-403

Dr. Fred's MIRACLE RUB

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 
histamine dihydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-403
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HISTAMINE DIHYDROCHLORIDE (HISTAMINE) HISTAMINE DIHYDROCHLORIDE0.25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
WATER 
ARNICA MONTANA 
C13-14 ISOPARAFFIN 
CETEARYL OLIVATE 
DIMETHYL SULFONE 
LAURETH-7 
MAGNESIUM SULFATE, UNSPECIFIED 
POTASSIUM SORBATE 
ROYAL JELLY 
SODIUM BENZOATE 
SODIUM STEARATE 
SORBITAN OLIVATE 
STEARIC ACID 
TROLAMINE 
Packaging
#Item CodePackage Description
1NDC:65121-403-251 BOTTLE in 1 CARTON
1118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/06/2013
Labeler - Pure Source, LLC (080354456)
Establishment
NameAddressID/FEIOperations
Pure Source, LLC080354456manufacture(65121-403)

 
Pure Source, LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.