ANTI-ITCH- camphor 0.5% menthol 0.5% lotion

Anti-Itch by

Drug Labeling and Warnings

Anti-Itch by is a Otc medication manufactured, distributed, or labeled by Meijer, Product Quest Mfg. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients                                  Purpose
Camphor 0.5%.......................................External Analgesic
Menthol 0.5%.........................................External Analgesic

PURPOSE

INDICATIONS & USAGE

Uses

For temporary relief of pain and itching associated with
minor burns sunburn minor cuts scrapes insect bites
minor skin irritations

WARNINGS

Warnings
For external use only
When using this product Avoid contact with the eyes.
Stop use and ask a doctor if Condition worsens Symptoms persist
for more than 7 days or clear up and occur again within a few days.
Keep out of reach of children. If swallowed, get medical help or contact
a Poison Control Center right away

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION

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: Consult a doctor.

Inactive ingredients

Carbomer
Cetyl Alcohol
DMDM Hydantoin
Fragrance
Glyceryl Stearate
Isopropyl Myristate
PEG-8 Stearate
PEG-100 Stearate
Petrolatum
Sodium Hydroxide
Stearic Acid
Water

Questions? 866-483-2846

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTI-ITCH 
camphor 0.5% menthol 0.5% lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41250-797
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	0.5 g  in 100 mL
Menthol (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	Menthol	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
Cetyl Alcohol (UNII: 936JST6JCN)
DMDM Hydantoin (UNII: BYR0546TOW)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
Isopropyl Myristate (UNII: 0RE8K4LNJS)
PEG-8 Stearate (UNII: 2P9L47VI5E)
PEG-100 Stearate (UNII: YD01N1999R)
Petrolatum (UNII: 4T6H12BN9U)
Sodium Hydroxide (UNII: 55X04QC32I)
Stearic Acid (UNII: 4ELV7Z65AP)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41250-797-06	222 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/02/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	07/02/2012

Labeler - Meijer (006959555)

Registrant - Product Quest Mfg (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg		927768135	manufacture(41250-797) , label(41250-797)