HEB 218.002/218AF Clear Anti-Itch Lotion

Manufacturer
H E B | Nice-Pak Products, LLC
Effective date
2026-06-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-07-17 21:35:27

Label at a glance#

ProductCLEAR ANTI ITCH
Active ingredientPRAMOXINE HCL, ZINC ACETATE
Label structure14 sections

Indications and 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

Dosage and administration

shake well before applying wash 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: ask a doctor

Storage and handling

store at room temperature 59°-77°F (15°–25°C)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Pramoxine HCl 1%

Zinc acetate 0.1%

Purpose

OTC - PURPOSE SECTION

External analgesic

Skin protectant

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well
  • before applying wash 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: ask a doctor

Other information

STORAGE AND HANDLING SECTION

store at room temperature 59°-77°F (15°–25°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

1-888-593-0593

Disclaimer

SPL UNCLASSIFIED SECTION

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

Adverse Reaction

ADVERSE REACTIONS SECTION

MADE WITH PRIDE & CARE FOR H-E-B ®

SAN ANTONIO, TX 78204

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to Caladryl ® Clear ®*

H-E-B ®

Clear Anti-Itch Lotion

External Analgesic/Skin Protectant

  • Relieves pain & itching caused by: poison ivy, poison sumanc, poison oak, and insect bites
  • Dries Clear

6 FL OZ (177 mL)

mm01mm01

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59640-21859640-218-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CLEAR ANTI ITCHPRAMOXINE HCL, ZINC ACETATE LOTIONH E B54f04056-d805-8c62-e063-6394a90ab7402026-06-23Warnings, Adverse reactionsExact identifier
ndc (package): 59640-218-30
ndc (product): 59640-218
ndc11 (package): 59640021830
spl id: 54f04056-d806-8c62-e063-6394a90ab740
spl set id: 54f04056-d805-8c62-e063-6394a90ab740

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.