Dosage and administration
wet hands with water first, then take appropriate hand sanitizer in the hands to scrub,finally rinse with water.
Air raid card Antibacterial Hand Sanitizer
- Manufacturer
- Jiangsu Manwei Pharmaceutical Co.,Ltd
- Effective date
- 2020-05-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:32:08
Label at a glance#
ProductAir raid card Antibacterial Hand Sanitizer
Active ingredientCHLOROXYLENOL, SALICYLIC ACID
Label structure12 sections
Storage and handling
Store in a cool and ventilated place,
Label contents#
Full prescribing information#
Active Ingredient(s)
CHLOROXYLENOL 0.3%,SALICYLIC ACID 0.5%.
Purpose
Antiseptic, Hand Sanitizer
scope of application
applicable to hand hygiene
OTC - WHEN USING SECTION
wet hands with water first, then take appropriate hand sanitizer in the hands to scrub,finally rinse with water.
Matters needing attention
This product is for external use only.
Do not use
It is forbidden to be taken orally. It is forbidden for people allergic to this product
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Do not use for children under 3 years old
Directions
wet hands with water first, then take appropriate hand sanitizer in the hands to scrub,finally rinse with water.
Other information
Store in a cool and ventilated place,
Inactive ingredients
PROPYLENE GLYCOL,
ETHYL BENZOATE,
EDETATE DISODIUM ANHYDROUS,
BENZYL ALCOHOL,
GLYCOSINE,
2-(METHYLAMINO)ETHANOL,
SODIUM CHLORIDE,
WATER,
SODIUM LAURETH-3 SULFATE,
POTASSIUM HYDROXIDE
Package Label - Principal Display Panel
Products#
Every source-derived product name is available through these pages.
- Air raid card Antibacterial Hand Sanitizer
- CHLOROXYLENOL
- SODIUM LAURETH-3 SULFATE
- WATER
- SALICYLIC ACID
- PROPYLENE GLYCOL
- POTASSIUM HYDROXIDE
- METHYL BENZOATE
- EDETATE DISODIUM ANHYDROUS
- BENZYL ALCOHOL
- GLYCOSINE
- 2-(METHYLAMINO)ETHANOL
- SODIUM CHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 75086-017 | 75086-017-01, 75086-017-02, 75086-017-03, 75086-017-04, 75086-017-05, 75086-017-06, 75086-017-07, 75086-017-08 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CHLOROXYLENOL | 0F32U78V2Q | ACTIB |
| SODIUM LAURETH-3 SULFATE | BPV390UAP0 | IACT |
| WATER | 059QF0KO0R | IACT |
| SALICYLIC ACID | O414PZ4LPZ | ACTIB |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| POTASSIUM HYDROXIDE | WZH3C48M4T | IACT |
| METHYL BENZOATE | 6618K1VJ9T | IACT |
| EDETATE DISODIUM ANHYDROUS | 8NLQ36F6MM | IACT |
| BENZYL ALCOHOL | LKG8494WBH | IACT |
| GLYCOSINE | D5JUH3HNWF | IACT |
| 2-(METHYLAMINO)ETHANOL | ZMQ4G4V497 | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| a52460b4-1bb1-521a-e053-2995a90ad217 | a52591f0-7f38-280e-e053-2a95a90ad0bd | 2020-05-08 | Warnings | a52460b4-1bb1-521a-e053-2995a90ad217 a52591f0-7f38-280e-e053-2a95a90ad0bd |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.