FDA.reportPublic FDA data

Australian Dream Carpal Tunnel Pain Cream

Manufacturer
Nature's Health Connection
Effective date
2019-10-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:03:12

Label at a glance#

ProductAustralian Dream Carpal Tunnel Pain
Active ingredientHISTAMINE DIHYDROCHLORIDE
Label structure9 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints aasocillled 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.

Storage and handling

Store between 40°F and 86°F (4°C and 30°C). Tamper Evident Feature: do not use if outer shrink wrap on jar is torn, broken or missing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Histamine Dihydrochloride 0.025%

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.

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

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

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

STORAGE AND HANDLING SECTION

  • Store between 40°F and 86°F (4°C and 30°C).
  • Tamper Evident Feature: do not use if outer shrink wrap on jar is torn, broken or missing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe Vera Gel)
Juice, Aqua (Deionized Water, Ascoriblc
Acid (Vitamin C), Butylene Glycol,
Camellia Sinensis (Green Tea) Leaf
Extract, Chamomilla Recutita
(Matricaria) flower Extract, Emu 011,
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 Soribate,
Punica Granatum (Pomegranate}
Extract, Saccharide lsomerate, Sodium
Polyacrylate, Tocopheryl Acetate
(Vrtamin E), Trideceth-6, Vaccinium
Angustifolium (Bluebeny) Fruit Extract,
Zemea (Corn) Propanedlol

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1.888.600.4642

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Australian Dream Cream Carpal TunnelAustralian Dream Cream Carpal Tunnel

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76017-76976017-769-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
INDIAN FRANKINCENSE4PW41QCO2MIACT
BROMELAINSU182GP2CF3IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
MATRICARIA RECUTITAG0R4UBI2ZZIACT
WATER059QF0KO0RIACT
EMU OIL344821WD61IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
REISHITKD8LH0X2ZIACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
LAURETH-7Z95S6G8201IACT
MAGNESIUM SULFATE, UNSPECIFIEDDE08037SABIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
NIACIN2679MF687AIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
EDETATE SODIUMMP1J8420LUIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TRIDECETH-63T5PCR2H0CIACT
TURMERIC856YO1Z64FIACT
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
98d2918a-a82e-2dfb-e053-2995a90a5d6c433d86c2-c2cc-07fd-e054-00144ff88e882019-12-03WarningsExact identifier
spl set id: 433d86c2-c2cc-07fd-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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