GOLDEN SUNSHINE HERBAL- topical analgesic spray 
Golden Sunshine International, Inc.

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Golden Sunshine Herbal Spray

Topical Analgesic

Active Ingredients

Menthol 0.8% - Topical Analgesic, Wintergreen Oil 0.3% - Topical Analgesic

Indications

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

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Directions

Hold can upright and spray until wet. Apply to clean and dry affected area 2 to 3 times daily as needed. Consult with a doctor for children under 6 years of age. 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.
  • In case of ingestion, seek professional assistance or contact a Poison Control Center immediately.
  • Do not expose to heat or store at temperature above 120 degrees F.

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

  • Keep out of reach of children.

Other Ingredients

Ethanol, lycopodii serrati herba, pseudoginseng radix, zingiber rhizoma, angelica dahuricae radix, paeoniae rubra radix, cinnamonomi cortex, jasmine oil.

For Questions or Comments Call:

1 (800) 798-3977

Golden Sunshine Herbal Spray sleeve for 120ml can.

GS Herbal Spray Sleeve.jpg

GOLDEN SUNSHINE HERBAL 
topical analgesic spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67475-114
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL.00781 g  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE.03 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M) .8197 g  in 1 g
HUPERZIA SERRATA (UNII: TLA53E5A4T) .016 g  in 1 g
PANAX PSEUDOGINSENG ROOT (UNII: NMK0ZS613U) .016 g  in 1 g
ZINGIBER MONTANUM ROOT (UNII: 3NG517NPD8) .016 g  in 1 g
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972) .008 g  in 1 g
PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P) .008 g  in 1 g
CHINESE CINNAMON (UNII: WS4CQ062KM) .004 g  in 1 g
JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432) .004 g  in 1 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67475-114-0120 in 1 BOX08/02/2004
11 in 1 BOX
1105 g in 1 CAN; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2NDC:67475-114-024000 g in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)08/02/2004
3NDC:67475-114-037 g in 1 VIAL; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)08/02/2004
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01708/02/200412/29/2022
Labeler - Golden Sunshine International, Inc. (098930857)
Registrant - Golden Sunshine International, Inc. (098930857)
Establishment
NameAddressID/FEIBusiness Operations
Golden Sunshine International, Inc.098930857label(67475-114)

Revised: 11/2023
Document Id: 1c56d827-62e9-4d58-b2af-ae66d08588c3
Set id: 8278a46c-2794-4ee4-b508-717db561a0be
Version: 3
Effective Time: 20231114
 
Golden Sunshine International, Inc.