1ST RELIEF TOPICAL- lidocaine and menthol spray 
1st Class Pharmaceuticals, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by 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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1st Relief Topical

ACTIVE INGREDIENT:

Lidocaine 4.00%

Menthol 1.00%

Topical Analgesic

Topical Analgesic

Indications:

For temporary relieft of pain associated with minor burns, minor cuts, scrapes, insect bites or skin irritations.

Warnings:

Keep out of reach of children.

If swallowed, conslut physician.

Directions

Other Ingredients:

Aqua (Deionized Water), ARNICA MONTANA,BOSWELLIA SERRATA, CETYL MYRISTOLEATE, EMU OIL, GLYCYRRHIZA GLABRA, METHYLSULFONYLMETHANE (MSM), POLYSORBATE 20, POTASSIUM SORBATE, SD-Alcohol 40B, SODIUM BENZOATE

If pregnant or breast feeding, contact physician prior to use.

Package Label

NDC 69094-226-04

1st Class

PHARMACEUTICALS INC.

1st RELIEF

TOPICAL SPRAY

For temporary relief of:

 • backache • bruises • arthritis • sprains

4 Fl OZ. (118 ml)

Distributed by:

1st Class PHARMACEUTICALS INC.

Los Angeles, CA 90064

www.1stclass pharmaceuticals.com

Label

1ST RELIEF TOPICAL 
lidocaine and menthol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69094-226
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ)  
CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)  
EMU OIL (UNII: 344821WD61)  
GLYCYRRHIZA GLABRA LEAF (UNII: GH32M797Y9)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69094-226-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product12/02/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34812/02/2014
Labeler - 1st Class Pharmaceuticals, Inc. (079448685)

Revised: 12/2017
Document Id: 616bfbf4-fa56-0956-e053-2a91aa0a24c6
Set id: e82e1df8-d722-4acf-b907-f8f50b242710
Version: 5
Effective Time: 20171228
 
1st Class Pharmaceuticals, Inc.