zanilast+ gel 70% alcohol

zanilast+ gel 70% alcohol
SPL v2
SPL
SPL Set ID aa19e8fd-302e-fe93-e053-2995a90aa870
Route
topical
Published
Effective Date 2020-07-10
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
alcohol (70 mL)
Inactive Ingredients
zinc oxide carbomer 940 glycerin limonene, (+)- water trolamine pyrithione zinc

Identifiers & Packaging

Marketing Status
otc monograph not final active Since 2020-07-10
Description

Ethyl Alcohol 70%

Medication Information

Warnings

For external use only. Flammable. Keep away from heat or flame

Directions
  • Wet hands thoroughly with product and allow to dry without wiping
Other Information
  • Store between 59-86ºF (15-30ºC)
  • Avoid freezing and excessive heat above (40ºC) 104ºF
Inactive Ingredients

Carbomer, glycerin, fragrance, triethanolamine, water, zinc oxide, zinc pyrithione

Description

Ethyl Alcohol 70%

Use

For hand washing to decrease bacteria on the skin.

Section 50565-1

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9

Stop use and ask a doctor if irritation and redness develop. Condition persists for more than 72 hours.

Section 51945-4

200000 mL NDC 69912-009-06

60 mL NDC 69912-009-05

500 mL NDC 69912-009-03

250 mL NDC 69912-009-04

Section 55105-1

Purpose: Antiseptic

Do Not Use
  • in the eyes
Active Ingredients

Ethyl Alcohol 70%

Structured Label Content

Warnings

For external use only. Flammable. Keep away from heat or flame

Directions
  • Wet hands thoroughly with product and allow to dry without wiping
Other Information (Other information)
  • Store between 59-86ºF (15-30ºC)
  • Avoid freezing and excessive heat above (40ºC) 104ºF
Inactive Ingredients (Inactive ingredients)

Carbomer, glycerin, fragrance, triethanolamine, water, zinc oxide, zinc pyrithione

Use

For hand washing to decrease bacteria on the skin.

Section 50565-1 (50565-1)

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9 (50566-9)

Stop use and ask a doctor if irritation and redness develop. Condition persists for more than 72 hours.

Section 51945-4 (51945-4)

200000 mL NDC 69912-009-06

60 mL NDC 69912-009-05

500 mL NDC 69912-009-03

250 mL NDC 69912-009-04

Section 55105-1 (55105-1)

Purpose: Antiseptic

Do Not Use (Do not use)
  • in the eyes
Active Ingredients

Ethyl Alcohol 70%

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

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Source: dailymed · Ingested: 2026-02-15T11:58:10.944251 · Updated: 2026-03-14T22:57:36.066065