FDA.reportPublic FDA data

Australian Dream Hand & Wrist Pain Cream

Manufacturer
Nature’s Health Connection, Inc.
Effective date
2017-06-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:15:15

Label at a glance#

ProductAustralian Dream Hand and Wrist Pain
Active ingredientHISTAMINE DIHYDROCHLORIDE
Label structure8 sections

Indications and uses

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

Dosage and administration

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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Histamine Dihydrochloride 0.025%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

  • For external use only.

Do not use 

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

  • 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, 

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

SPL UNCLASSIFIED SECTION

  • 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

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

Call 1.888.600.4642

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76017-83676017-836-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CHAMOMILEFGL3685T2XIACT
EMU OIL344821WD61IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
HELIANTHUS ANNUUS FLOWERING TOPBKJ0J3D1BPIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
MAGNESIUM SULFATE, UNSPECIFIED FORMDE08037SABIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
POMEGRANATE56687D1Z4DIACT
SACCHARIDE ISOMERATEW8K377W98IIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
TRIDECETH-63T5PCR2H0CIACT
LOWBUSH BLUEBERRYG90PX41VP0IACT
CORN0N8672707OIACT
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
98d2a73c-9aa5-7249-e053-2a95a90acd40531ff07b-f21c-293d-e054-00144ff8d46c2019-12-03WarningsExact identifier
spl set id: 531ff07b-f21c-293d-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.