DR. FREDS MIRACLE RUB- histamine dihydrochloride cream 
Pure Source, LLC

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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)

Label

DR. FREDS MIRACLE RUB 
histamine dihydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-403
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE0.25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
ARNICA MONTANA (UNII: O80TY208ZW)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
LAURETH-7 (UNII: Z95S6G8201)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
ROYAL JELLY (UNII: L497I37F0C)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM STEARATE (UNII: QU7E2XA9TG)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65121-403-251 in 1 CARTON02/09/2017
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01706/06/2013
Labeler - Pure Source, LLC (080354456)
Establishment
NameAddressID/FEIBusiness Operations
Pure Source, LLC080354456manufacture(65121-403)

Revised: 11/2023
Document Id: 0973aae6-55dc-5f1a-e063-6394a90a9848
Set id: 3801584a-6212-4ad0-8d6e-ef60e7edae14
Version: 5
Effective Time: 20231105
 
Pure Source, LLC