CLEAR ANTI-ITCH- pramoxine hcl, zinc acetate lotion

Clear Anti-Itch by

Drug Labeling and Warnings

Clear Anti-Itch by is a Otc medication manufactured, distributed, or labeled by Rite Aid, Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Pramoxine HCl 1%
Zinc acetate 0.1%

Purpose

External analgesic
Skin protectant

Uses

for the temporary relief of pain and itching associated with minor skin
 irritations and rashes due to poison ivy, poison oak, or poison sumac
dries the oozing and weeping of poison: ivy oak sumac

Warnings

For external use only

When using this product

do not get into eyes

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.

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

Directions

shake well  before applying wash affected area of skin
adults and children 2 years of age and older - apply to affected area no more than 3 to 4 times daily
children under 2 years - ask a doctor

Other information

store at room temperature (59⁰ - 77⁰ F)

Inactive ingredients

alcohol, camphor, citric acid, diazolidinyl urea, fragrance, glycerin, hypromellose, methylparaben, oil of lavender, oil of rosemary, polysorbate 40, propylene glycol, propylparaben, purified water, sodium citrate

Adverse reaction

*This product is not manufactured or distributed by Pfizer Consumer HealthCare, distributor of Caladryl Clear Lotion.

DISTRIBUTED BY: RITE AID
30 HUNTER LANE
CAMP HILL, PA17011

principal display panel

INGREDIENTS AND APPEARANCE

CLEAR ANTI-ITCH 
pramoxine hcl, zinc acetate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-0219
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 1 mL
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC ACETATE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
GLYCERIN (UNII: PDC6A3C0OX)
HYPROMELLOSES (UNII: 3NXW29V3WO)
METHYLPARABEN (UNII: A2I8C7HI9T)
LAVENDER OIL (UNII: ZBP1YXW0H8)
ROSEMARY OIL (UNII: 8LGU7VM393)
POLYSORBATE 40 (UNII: STI11B5A2X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-0219-6	177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/16/1997

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	10/16/1997

Labeler - Rite Aid (014578892)

Registrant - Humco Holding Group, Inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc.		825672884	manufacture(11822-0219) , analysis(11822-0219) , label(11822-0219)