Glucosamine cream extra strength cream

Drug facts

A ctive ingredient

Histamine Dihydrochloride 0.05%


Topical Analgesic

Indications & usage section

Uses For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains

Warnings section

Warnings For external use only

When using this product

  • Avoid contact with eyes
  • Do not bandage tightly

Do not use

  • On wounds or damaged skin or if you are allergic to ingredients in this product.

Discontinue use and consult a physician if: Condition worsens or if symptomspersists for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

If swallowed get medical help or contact a poison control center


For use by adults and children over 12 years:

Apply to affected area not more than 3 to 4 times daily.

Inactive ingredient section

Inactive ingredients Deionized water, cetearyl alcohol, emu oil, glycerine, ceteareth-20, glucosamine sulfate, dimethyl sulfone, caprylic capric triglyceride, phenoxyethanol, cetyl alcohol, methyl paraben, tocopherol acetate, butylene glycol, propylene glycol, chamomilla recutita flower extract,rosmarinus officinalis leaf extract,boswellia serrata extract, propyl paraben

Spl unclassified section

Pain Relief On Contact

Dual Action Moisturizing Cream

Odorless, Greaseless, Stainless.

Made in USA

For re-orders call 800-280-5590

Distributed by

Dr. Newton's Naturals

26 Thomas Drive

Westbrook, ME 04092

Ingredients and appearance - Product information

Glucosamine cream extra strength cream- Histamine dihydrochloride

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 52099-0008
Route of Administration Topical

Active Ingredient/Active Moiety

Ingredient Name Strength
Histamine dihydrochloride ( UNII: 3POA0Q644U)( Histamine - UNII: 820484N8I3 ) 0.05 gin 100 g

Inactive Ingredients

Ingredient Name Code
Water ( UNII: 059QF0KO0R)
Cetostearyl alcohol ( UNII: 2DMT128M1S)
Emu oil ( UNII: 344821WD61)
Glycerin ( UNII: PDC6A3C0OX)
Polyoxyl 20 cetostearyl ether ( UNII: YRC528SWUY)
Glucosamine sulfate ( UNII: 1FW7WLR731)
Dimethyl sulfone ( UNII: 9H4PO4Z4FT)
Medium-chain triglycerides ( UNII: C9H2L21V7U)
Phenoxyethanol ( UNII: HIE492ZZ3T)
Cetyl alcohol ( UNII: 936JST6JCN)
Methylparaben ( UNII: A2I8C7HI9T)
.alpha.-tocopherol acetate ( UNII: 9E8X80D2L0)
Butylene glycol ( UNII: 3XUS85K0RA)
Propylene glycol ( UNII: 6DC9Q167V3)
Chamomile ( UNII: FGL3685T2X)
Rosemary ( UNII: IJ67X351P9)
Indian frankincense ( UNII: 4PW41QCO2M)
Propylparaben ( UNII: Z8IX2SC1OH)

Product Characteristics

Color white

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC monograph not final part348 USA

Labeler - Q.A. Laboratories( 065361149)


Name ID/FEI Business Operations
Q.A. Laboratories 065361149 manufacture( 52099-0008)