STILL STANDING- menthol, unspecified form liquid 
Natural Essentials 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.

----------

Drug Facts

Active Ingredients

Menthol 10%

Purpose

Topical analgesic

Uses

For temporary relief of minor pain of muscles and joints associated with:

Warnings

For external use only

Flammable:

Do not apply

  • to wounds or damaged, broken or irritated skin.
  • Do not allow contact with eyes or mucous membranes.

When using this product

  • keep out of eyes
  • do not bandage tightly
  • do not use with a heating pad
  • use only as directed
  • do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or dear up and occur again within a few days
  • needed for longer than a week

If pregnant or breast-feeding

  • ask a health professional before use.

Keep out of reach of children and pets.

  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive Ingredients

Alcohol Denatured, Aloe Barbadensis Leaf Juice Powder, Arnica Montana Flower Extract, Camphor, Citric Acid, Ilex Paraguariensis Leaf Extract, Melaleuca Altemifolia (Tea Tree) Leaf Oil, Methyl Salicylate, Tocopherol, Water

Questions/Comments

www.stillstandingspray.com

Principal Display Panel – 15 mL Bottle Spray Label

STILL
STANDING®

FOOT SPRAY

0.5 fl oz (15 mL)

Principal Display Panel – 15 mL Bottle Spray Label

Principal Display Panel – 15 mL Bottle Spray Label

STILL
STANDING®

FOOT SPRAY

UNISEX

0.5 fl oz (15 mL)

Principal Display Panel – 15 mL Bottle Spray Label

Principal Display Panel – 18 mL Bottle Spray Label

STILL
STANDING

UNISEX®

0.60 fl oz (18 mL)

Principal Display Panel – 18 mL Bottle Spray Label
STILL STANDING 
menthol, unspecified form liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66902-167
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM89 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
TEA TREE OIL (UNII: VIF565UC2G)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66902-167-1515 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/28/2023
2NDC:66902-167-1715 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/28/2023
3NDC:66902-167-1818 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/28/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/28/2023
Labeler - Natural Essentials Inc. (947484713)
Establishment
NameAddressID/FEIBusiness Operations
NATURAL ESSENTIALS, INC.947484713MANUFACTURE(66902-167)

Revised: 2/2023
Document Id: 4f69e04c-9c6f-4364-bc0e-012af7336076
Set id: 66974aaf-c82f-4fe9-bfb3-3430b80ac9f2
Version: 1
Effective Time: 20230228
 
Natural Essentials Inc.