PAIN AWAY- analgesic spray 
Eagle Labs Inc.

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Pain Spray Extra Strength

ACTIVE INGREDIENT

Capsacin; Analgesic

Menthol: Analgesic

Camphor: Analgesic

PAIN RELIEF - TOPICAL ANALGESIC

Analgesic

Indications

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

Simple backache
Arthritis
Strains
Bruises
Sprains

Warnings

Stop use and consult a doctor if:

When using this product

  • Use only as directed
  • Do not apply heat (heating pads) or apply patches to area

Keep out of children

If accidentally swallowed get medical help or contact a poison control center immediately

If pregnant or breastfeeding

If pregnant or breastfeeding, ask a health professional before use.

Keep out of the reach o children

If accidentally swallowed get medical help or contact a poison control center immediately

Flammable

Keep away from excessive heat or open flame

Flammable

Keep away from excessive heat or open flame

Inactive Ingredients

Isopropanol, MCT, Phenoxyethanol, Simethicone

Directions

Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age consult a doctor.

Pain Relief Pro

Pain Relief Pro

Insta Eaze Spray the Pain Away

Insta Eaze Spray the Pain Away

PAIN AWAY 
analgesic spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79804-265
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.16 g  in 1 g
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.001 g  in 1 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)0.11 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
PALM OIL (UNII: 5QUO05548Z)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79804-265-04108 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2022
2NDC:79804-265-08216 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01707/01/2022
Labeler - Eagle Labs Inc. (118496872)
Registrant - Eagle Labs Inc (118496872)
Establishment
NameAddressID/FEIBusiness Operations
Eagle Labs Inc118496872manufacture(79804-265) , label(79804-265) , pack(79804-265)

Revised: 4/2024
Document Id: 16234cb9-8435-02c9-e063-6294a90a6d05
Set id: 3de88c3b-0302-4005-8029-98364c6257f7
Version: 4
Effective Time: 20240415
 
Eagle Labs Inc.