STILL STANDING- menthol, unspecified form liquid

Still Standing by

Drug Labeling and Warnings

Still Standing by is a Otc medication manufactured, distributed, or labeled by Natural Essentials Inc., NATURAL ESSENTIALS, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Menthol 10%

Purpose

Topical analgesic

Uses

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

• arthritis
• simple backache
• strains
• bruises
• sprains

Warnings

For external use only

Flammable:

• Do not use while smoking or near heat or flame

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

• shake well
• adults and children 12 years of age and olden
• spray product on area not more than 1 to 3 times daily
• children under 12 years of age ■ask a doctor

Other information

• May cause staining. Use with caution when spraying near fabric and unprotected surfaces

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

STILL
STANDING®

FOOT SPRAY

UNISEX

0.5 fl oz (15 mL)

Principal Display Panel – 18 mL Bottle Spray Label

STILL
STANDING

UNISEX®

0.60 fl oz (18 mL)

INGREDIENTS AND APPEARANCE

STILL STANDING 
menthol, unspecified form liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66902-167
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	89 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66902-167-15	15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/28/2023
2	NDC: 66902-167-17	15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/28/2023
3	NDC: 66902-167-18	18 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/28/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/28/2023

Labeler - Natural Essentials Inc. (947484713)

Establishment
Name	Address	ID/FEI	Business Operations
NATURAL ESSENTIALS, INC.		947484713	manufacture(66902-167)