Australian Dream Hand & Wrist Pain Cream

Australian Dream Hand and Wrist Pain by

Drug Labeling and Warnings

Australian Dream Hand and Wrist Pain by is a Otc medication manufactured, distributed, or labeled by Nature’s Health Connection, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

AUSTRALIAN DREAM HAND AND WRIST PAIN- histamine dihydrochloride cream 
Nature’s Health Connection, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Australian Dream Hand & Wrist Pain Cream

Drug Facts

Active ingredient

Histamine Dihydrochloride 0.025%

Purpose

Topical Analgesic

Uses

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

Warnings

  • For external use only.

Do not use 

  • on wounds or damaged skin or if you are allergic to ingredients in the product.

When using this product

  • avoid contact with eyes. if product gets into eyes, rinse thoroughly with water.
  • do not bandage tightly or use a heating pad.

Stop use and ask a doctor if

  • rash appears.
  • condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and occur again within a few days.

If pregnant or breast feeding, 

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • For use by Adults and Children over 12 years.
  • Apply a thin layer to pain site and massage until thoroughly absorbed into skin. Apply no more than 3 to 4 times daily.
  • Children 12 years or younger consult a physician.

Other information

  • Store between 40°F and 86°F (4° C and 30°C).
  • Tamper Evident Feature: do not use if seal under cap is torn, broken or missing.

Inactive ingredients

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water, Ascorbic Acid (Vitamin C), Butylene Glycol, Camellia Sinensis (Green Tea) Leaf Extract, Chamomilla Recutita (Matricaria) flower Extract, Emu Oil, Ethylhexylglycerin, Ethylhexyl Stearate, Glycyrrhiza Glabra (licorice) Root Extract, Helianthus Annuus (Sunflower) Seed Oil, C13-14 Isoparaffin, L.aureth-7, Magnesium Sulfate, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Potassium Sorbate, Punica Granatum (Pomegranate) Extract, Saccharide Isomerate, Sodium Polyacrylate, Tocopheryl Acetate (Vitamin E), Trideceth-6, Vaccinium Angustifolium (Blueberry) Fruit Extract, Zemea (Corn) Propanedlol

Questions or Comments?

Call 1.888.600.4642

Package Labeling:

Label2

AUSTRALIAN DREAM HAND AND WRIST PAIN 
histamine dihydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76017-836
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE0.25 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
CHAMOMILE (UNII: FGL3685T2X)  
EMU OIL (UNII: 344821WD61)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
POMEGRANATE (UNII: 56687D1Z4D)  
SACCHARIDE ISOMERATE (UNII: W8K377W98I)  
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
LOWBUSH BLUEBERRY (UNII: G90PX41VP0)  
CORN (UNII: 0N8672707O)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76017-836-011 in 1 BOX06/28/201712/03/2019
1119 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/28/201712/03/2019
Labeler - Nature’s Health Connection, Inc. (079549213)

Revised: 12/2019
Document Id: 98d2a73c-9aa5-7249-e053-2a95a90acd40
Set id: 531ff07b-f21c-293d-e054-00144ff8d46c
Version: 2
Effective Time: 20191203