Solimo 218.002/218AF Clear Anti-Itch Lotion

Clear Anti Itch by

Drug Labeling and Warnings

Clear Anti Itch by is a Otc medication manufactured, distributed, or labeled by Amazon.Com Services LLC, Vi-Jon Inc, Vi-Jon, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CLEAR ANTI ITCH- pramoxine hcl, zinc acetate lotion 
Amazon.Com Services LLC

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Solimo 218.002/218AF
Clear Anti-Itch Lotion

Active Ingredients

Pramoxine HCl 1%

Zinc acetate 0.1%

Purpose

External analgesic

Skin protectant

Use

• 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 was affected area of skin

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

Other information

store at room temperature (59°-77°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

DISTRIBUTED BY:

Amazon.com, Services, Inc

Seattle, WA 98109

1-877-485-0385

2018 Amazon.com, Inc. or its afiliated.

All rights reserved. Solimo and all related logos are are trademarks of Amazon.com, Inc or its affiliates.

principal display panel

SOLIMO

Medicated Calamine Lotion

EXTERNAL ANALGESIC

SKIN PROTECTANT

Anti-itch lotion

6 FL OZ (177 mL)

CLEAR ANTI ITCH 
pramoxine hcl, zinc acetate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72288-218
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 CATION	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
BENZOIC ACID (UNII: 8SKN0B0MIM)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
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: 72288-218-30	177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2018	07/12/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	05/01/2018	07/12/2024

Labeler - Amazon.Com Services LLC (128990418)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(72288-218)

Revised: 9/2024

Document Id: 21ecf974-b30f-bde0-e063-6294a90ad600

34390-5

Set id: e10fd91c-60df-41d1-accd-fc9aed8d8354

Version: 4

Effective Time: 20240912