Indications and uses
For hand sanitizing to decrease bacteria on the skin
Sipa Foaming Hand Sanitizer Alcohol Free
- Manufacturer
- LMZ (Jiangsu) Industrial Co.,Ltd
- Effective date
- 2021-01-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:56:11
Label at a glance#
ProductSipa Foaming Hand Sanitizer Alcohol Free
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections
Label contents#
Full prescribing information#
Active ingredient
Benzalkonium chloride 0.15%
Uses
For hand sanitizing to decrease bacteria on the skin
Warnings
For external use only
Do not use
Do not use in Or near the eyes
in case of contact,rinse eyes thoroughly with water
OTC - WHEN USING SECTION
Do not use in Or near the eyes
in case of contact,rinse eyes thoroughly with water
Stop use and ask a doctor if irritation or rash appears and lasts
Keep out of reach of children.If swallowed,get medical help or contact a Poison Control Center
Stop use and ask a doctor
Stop use and ask a doctor if irritation or rash appears and lasts
Keep out of reach of children
Keep out of reach of children.If swallowed,get medical help or contact a Poison Control Center
DOSAGE & ADMINISTRATION SECTION
Pump d small amount of foam into palm of hand
Rub thoroughly over all surfaces of both hands
Rub hands together briskly until dry
Inactive ingredients
Water, Didecyldimonium Chloride, Glycerin, Propylene Glycol, Peg-10 Dimethicone, Peg-17 Dimethicone, Phenoxyethanol
Package Label - Principal Display Panel
50ml 57816-010-01
60ml 57816-010-02
236ml 57816-010-04
250ml 57816-010-05
473ml 57816-010-07
502ml 57816-010-08
3780ml 57816-010-10
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- Sipa Foaming Hand Sanitizer Alcohol Free
- Instant Hand Sanitizer
- PHENOXYETHANOL
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- PROPYLENE GLYCOL
- DIDECYLDIMONIUM CHLORIDE
- WATER
- GLYCERIN
- PEG-10 DIMETHICONE (600 CST)
- PEG/PPG-17/18 DIMETHICONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 57816-010 | 57816-010-01, 57816-010-07, 57816-010-05, 57816-010-08, 57816-010-09, 57816-010-10, 57816-010-02, 57816-010-03, 57816-010-04, 57816-010-06 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| DIDECYLDIMONIUM CHLORIDE | JXN40O9Y9B | IACT |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| PEG-10 DIMETHICONE (600 CST) | 8PR7V1SVM0 | IACT |
| PEG/PPG-17/18 DIMETHICONE | 2E4ZJH3Z6R | 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 |
|---|---|---|---|---|---|---|
| f04ebd0f-56d5-df15-e053-2995a90a605a | b9016a0d-e336-c8bb-e053-2a95a90a9dad | 2022-12-20 | Warnings | b9016a0d-e336-c8bb-e053-2a95a90a9dad |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.