PROCURE ANTI ITCH- camphor 0.5% lotion

ProCure Anti Itch by

Drug Labeling and Warnings

ProCure Anti Itch by is a Otc medication manufactured, distributed, or labeled by Twin Med LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Camphor 0.5%

Purpose

External Analgesic

Uses

Uses

For the temporary relief of pain and itching associated with: nsect bites, minor cuts, minor burns, sunburn, scrapes, minor skin irritations, rashes due to poison ivy, poison oak, or poison sumac

Warnings

Warnings

For external use only

When using this product

When using this product avoid contact with the eyes

Stop use and ask a doctor if

Stop use and ask a doctor if

• Condition worsens
• Symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children

Keep out of reach of children. In case of accidental ingestion contact a physician or Poison Control Center right away.

Directions

Directions

• Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily
• Children under 2 years of age: do not use, consult a physician

Inactive Ingredients

Inactive Ingredients

Carbomer, Cetostearyl Alcohol, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Imidurea, Glycol Stearate, Menthol, Mineral Oil, PEG-40 Castor Oil, Petrolatum, Phenoxyethanol, Propylene Glycol, Sodium Cetostearyl Sulfate, Sodium Hydroxide, Stearic Acid, Titanium Dioxide, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROCURE ANTI ITCH 
camphor 0.5% lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55681-038
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
IMIDUREA (UNII: M629807ATL)
GLYCOL STEARATE (UNII: 0324G66D0E)
MINERAL OIL (UNII: T5L8T28FGP)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PETROLATUM (UNII: 4T6H12BN9U)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55681-038-75	222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/15/2025

Labeler - Twin Med LLC (009579330)