ITCH RELIEF MEDICATED PADS CVS- pramoxine hcl, zinc acetate liquid

Itch Relief Medicated Pads by

Drug Labeling and Warnings

Itch Relief Medicated Pads by is a Otc medication manufactured, distributed, or labeled by CVS, Product Quest Mfg, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Pramoxine  HCl 1%               External Analgesic

Zinc Acetate 0.1%                 Skin Pretectant

Uses

• Temporarily relieves pain and itching asociated with:
• rashes due to poison ivy, poison oak or poison sumac.
• insect bites.
• minor skin irritation.
• minor cuts.
• dries the oozing and weeping of poison ivy, poison oak and poison sumac.

Warnings

For external use only.

Flammable: Do not use near heat, flame, or while smoking.

​​​

When using this product

• keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

• condition worsens or does not improve within 7 days.

• symptoms persist for more than 7 days or clear up and occur again with in a few days.

Keep out of reach of children

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

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: ask a doctor. 

Inactive ingredients

Avena Sativa (Oat) Meal Extract
Camphor
Citric Acid
Diazolidinyl Urea
Fragrance
Glycerin
Hydroxypropyl Methylcellulose
Methylparaben
Polysorbate 40
Propylene Glycol
Propylparaben
SD Alcohol 38-B
Sodium Citrate
Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ITCH RELIEF MEDICATED PADS  CVS
pramoxine hcl, zinc acetate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-842
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
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC ACETATE	.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
OATMEAL (UNII: 8PI54V663Y)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
GLYCERIN (UNII: PDC6A3C0OX)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYSORBATE 40 (UNII: STI11B5A2X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-842-03	69 g in 1 JAR; Type 0: Not a Combination Product	03/15/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	03/15/2017

Labeler - CVS (062312574)

Registrant - Product Quest Mfg, LLC (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg, LLC		927768135	manufacture(69842-842)