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 CDMA, Consumer Product Partners, 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, benzoic acid, camphor, citric acid, fragrance, glycerin, hydroxypropyl methylcellulose, Lavandula angustifolia (lavender) oil, polysorbate 40, Rosmarinus officinalis (rosemary) leaf oil, sodium citrate, water

Disclaimer

*This product is not manufactured or distributed by Bausch Health US, LLC, distributor of Caladryl Clear Lotion.

ADVERSE REACTION

Distibuted by CDMA, Inc.

Novi, MI 48375

www.qualitychoice.com

Questions: 800-935-2362

SATISFACTION GUARANTEED

100% QC

PRINCIPAL DISPLAY PANEL

NDC: 83324-245-06

QC

QUALITY CHOICE

*Compare to CALADRYL CLEAR

Clear 

Anti-Itch

Lotion

External Analgesic/Skin Protectant

Relieves pain & itching caused by:

Poison Ivy, Poison Sumac, Poison Oak & Insect Bites

6 FL OZ (177 mL)

INGREDIENTS AND APPEARANCE

CLEAR ANTI-ITCH 
pramoxine hcl, zinc acetate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83324-245
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)
BENZOIC ACID (UNII: 8SKN0B0MIM)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
LAVENDER OIL (UNII: ZBP1YXW0H8)
POLYSORBATE 40 (UNII: STI11B5A2X)
ROSEMARY OIL (UNII: 8LGU7VM393)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83324-245-06	177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/26/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	02/26/2025

Labeler - CDMA (011920774)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(83324-245)