WALGREEN ANTI-ITCH- pramoxine hcl lotion

Walgreen Anti-Itch by

Drug Labeling and Warnings

Walgreen Anti-Itch by is a Otc medication manufactured, distributed, or labeled by Walgreens, Weeks & Leo, Inc., WEEKS & LEO COMPANY, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Pramoxine HCl 1% External analgesic

Uses

temporary relieves pain and itching due to:

insect bites

minor burns

sunburn

minor skin irritations

minor cuts

scrapes

rashes due to poison ivy, poison oak, and poison sumac

dries the oozing and weeping of poison:

ivy

oak

sumac

Warning

For external use only

Do not use

in the eyes or nose

over large areas of the body for prolonged periods

Ask doctor before use

on chicken pox

on measles

When using this product

do not get into eyes

Stop Use and ask 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

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

Purpose

Anti - itch

Directions

to open, squeeze cap tightly and turn pump counter-clockwise

adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily

children under 2 years: ask a doctor

Other information

store at 20 °C to 25 °C (68 °F to 77 °F)

Inactive ingredients

benzyl alcohol, carbomer 940, cetyl alcohol, dimethicone, glyceryl stearate, isopropyl myristate, PEG-40 stearate,
PEG-100 stearate, purified water, sodium hydroxide, stearic acid, white petrolatum

Principal Display Panel

Walgreens

Compare to Sarna Sensitive Anti-Itch Lotion

Sensitive Formula Anti-Itch Lotion

Pramoxine Hydrochloride 1 percent

Steroid Free

Reduces and Relieves Itching associated with eczema, dry and sensitive skin

INGREDIENTS AND APPEARANCE

WALGREEN ANTI-ITCH 
pramoxine hcl lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0263
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
DIMETHICONE 350 (UNII: 2Y53S6ATLU)
PEG-40 STEARATE (UNII: ECU18C66Q7)
CARBOMER 940 (UNII: 4Q93RCW27E)
PETROLATUM (UNII: 4T6H12BN9U)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0263-75	212 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/08/2020

Labeler - Walgreens (008965063)

Registrant - Weeks & Leo, Inc. (005290028)

Establishment
Name	Address	ID/FEI	Business Operations
WEEKS & LEO COMPANY, INC.		005290028	manufacture(0363-0263)