GLUCOSAMINE CREAM EXTRA STRENGTH- histamine dihydrochloride cream

Glucosamine Cream EXTRA STRENGTH by

Drug Labeling and Warnings

Glucosamine Cream EXTRA STRENGTH by is a Otc medication manufactured, distributed, or labeled by Q.A. Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Histamine Dihydrochloride 0.05%

Purpose

Topical Analgesic

INDICATIONS & USAGE

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

WARNINGS

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 symptoms persists 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

Directions

For use by adults and children over 12 years:

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

INACTIVE INGREDIENT

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

www.drnewtons.com

Distributed by

Dr. Newton's Naturals

26 Thomas Drive

Westbrook, ME 04092

Packaging

INGREDIENTS AND APPEARANCE

GLUCOSAMINE CREAM EXTRA STRENGTH 
histamine dihydrochloride cream

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	0.05 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52099-0008-3	85 g in 1 TUBE; Type 0: Not a Combination Product	04/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/01/2017

Labeler - Q.A. Laboratories (065361149)

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