Label: GOLDEN SUNSHINE FAR INFRARED HOT HERBAL- menthol and methyl salicylate patch
- NDC Code(s): 62699-1112-1, 62699-1112-2, 62699-1112-3
- Packager: Nan Mei Pharmaceutical Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
NOTE: Most over the counter (OTC) are not reviewed and approved by the 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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- Active Ingredients
Menthol 3% - Topical Analgesic, Wintergreen Oil 0.5% - Topical AnalgesicClose
For the temporary relief of minor aches of muscles and joints associated with:
- simple backache
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.Close
- 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.
- 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, tartrazineClose
- For Questions or Comments Call:
1 (800) 798-3977Close
- 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 LABEL Item Code (Source) NDC:62699-1112 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (MENTHOL) MENTHOL .03 g in 1 g METHYL SALICYLATE (SALICYLIC ACID) METHYL SALICYLATE .005 g in 1 g Inactive Ingredients Ingredient Name Strength SESAME OIL .565 g in 1 g PINUS MASSONIANA RESIN .2 g in 1 g NELUMBO NUCIFERA STAMEN .03 g in 1 g ZINC OXIDE .3 g in 1 g LIQUIDAMBAR ORIENTALIS RESIN .02 g in 1 g FRANKINCENSE .02 g in 1 g MYRRH .02 g in 1 g ANGELICA SINENSIS ROOT .014 g in 1 g SCROPHULARIA NINGPOENSIS ROOT .014 g in 1 g GLEDITSIA SINENSIS FRUIT .014 g in 1 g ANGELICA DAHURICA ROOT .014 g in 1 g PRUNUS ARMENIACA SEED .014 g in 1 g SCHORL TOURMALINE .01 g in 1 g FD&C YELLOW NO. 5 .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 1 3 in 1 POUCH 1 6 g in 1 PATCH 2 NDC:62699-1112-2 10 in 1 BAG 2 6 g in 1 PATCH 3 NDC:62699-1112-3 10 in 1 BAG 3 3 g in 1 PATCH 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 Mei Pharmaceutical Co., Ltd. (656348505)