GOLDEN SUNSHINE FAR INFRARED HOT HERBAL- topical analgesic patch

Golden Sunshine Far Infrared HOT Herbal by

Drug Labeling and Warnings

Golden Sunshine Far Infrared HOT Herbal by is a Otc medication manufactured, distributed, or labeled by Nan Me Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Topical Analgesic

Active Ingredients

Menthol 3% - Topical Analgesic, Wintergreen Oil 0.5% - Topical Analgesic

Indications

For the temporary relief of minor aches of muscles and joints associated with:

• simple backache
• arthritis
• strains
• bruises
• sprains

Directions

For adults and children 6 and older. Clean the affected area before use. Can be cut to size. Peel off film and cover affected area with patch. Keep on for up to 8 hours under normal conditions. Apply once or twice per day as needed. Allow skin to breath for a few hours between applications. Users with sensitive skin should test on a small area first.

Warnings

• FOR EXTERNAL USE ONLY

• Avoid contac with eyes or mucous membranes.
• Do not apply to wounds or damaged or irritated skin.
• Do not use if skin is sensitive, or have allergies to any ingredients in this product. Discontinue use and consult a doctor if signs of irritation or rash appear.
• Avoid use on extremely hairy areas of the body as removal may remove hair.

• If pregnant or breast feeding consult a doctor before use.

• Keep out of reach of children.

Other Ingredients

Sesame oil, resin, nelumbinis stamin, zinc oxide, resina liquidambaris, frankencense, myrrha, angelicae sinensis radix, scrophulariae radix, gleditsiae abnormalis fructus, angelicae dahuricae radix, armeniacae amarum semen, tourmaline, tartrazine

For Questions or Comments Call:

1 (800) 798-3977

Golden Sunshine Far Infrared HOT Herbal Patch pouch for 3 patches.

INGREDIENTS AND APPEARANCE

GOLDEN SUNSHINE FAR INFRARED HOT HERBAL 
topical analgesic patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62699-1112
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	.03 g  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	.005 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SESAME OIL (UNII: QX10HYY4QV)	.565 g  in 1 g
PINUS MASSONIANA RESIN (UNII: 64S07U83T7)	.2 g  in 1 g
NELUMBO NUCIFERA STAMEN (UNII: 88637P8Y3U)	.03 g  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z)	.3 g  in 1 g
LIQUIDAMBAR ORIENTALIS RESIN (UNII: 63V91G4W93)	.02 g  in 1 g
FRANKINCENSE (UNII: R9XLF1R1WM)	.02 g  in 1 g
MYRRH (UNII: JC71GJ1F3L)	.02 g  in 1 g
ANGELICA SINENSIS ROOT (UNII: B66F4574UG)	.014 g  in 1 g
SCROPHULARIA NINGPOENSIS ROOT (UNII: HC0FB6P85R)	.014 g  in 1 g
GLEDITSIA SINENSIS FRUIT (UNII: A6W0J6UO7Q)	.014 g  in 1 g
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)	.014 g  in 1 g
PRUNUS ARMENIACA SEED (UNII: 75356789IW)	.014 g  in 1 g
SCHORL TOURMALINE (UNII: 173O8XLY6T)	.01 g  in 1 g
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)	.0001 g  in 1 g

Product Characteristics
Color	yellow	Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62699-1112-1	50 in 1 BOX	08/02/2004
1		3 in 1 POUCH
1		6 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 62699-1112-2	10 in 1 BAG	08/02/2004
2		6 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3	NDC: 62699-1112-3	10 in 1 BAG	08/02/2004
3		3 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/02/2004

Labeler - Nan Me Pharmaceutical Co., Ltd. (656348505)