Drug Facts Box OTC-Active Ingredient Section
Benzalkonium Chloride 2.5%
All Stop Medicated Body Wash
- Manufacturer
- Q-Based Solutions Inc | ABC Compounding Co., Inc.
- Effective date
- 2019-07-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:19:13
Label at a glance#
ProductAll Stop Medicated Body Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections
Label contents#
Full prescribing information#
Drug Facts Box OTC-Purpose Section
Antiseptic
Drug Facts Box OTC-Indications & Usage Section
for hand-washing to decrease bacteria on the skin
Drug Facts Box OTC-Warnings Section
For external use only
Drug Facts Box OTC-When Using Section
do not get into eyes
if contact occurs, rinse eyes thoroughly with water
Drug Facts Box OTC-Stop Use Section
irritation and redness develop
Drug Facts Box OTC-Keep Out of Reach of Children Section
if swallowed, get medical help or contact a Poison Control Center right away
Drug Facts Box OTC-Dosage & Administration Section
- wet hands and forearms
- apply 5 milliliters (teaspoonful) or palmful to hands and forearms
- scrub thoroughly for 1 minute and rinse
Drug Facts Box OTC-Inactive Ingredient Section
ater, glycerin, isopropyl alcohol, disodium cocoamphodiproprionate, hydroxyethylcellulose, lauramine oxide,
PEG-75 lanolin, citric acid, FD and C red no.4
All Stop Medicated Body Wash 6265 Drug Facts and Label
All Stop Medicated Body Wash 6265 Drug Facts and Label
Products#
Every source-derived product name is available through these pages.
- All Stop Medicated Body Wash
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- WATER
- ISOPROPYL ALCOHOL
- HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%)
- DISODIUM COCOAMPHODIPROPIONATE
- LAURAMINE OXIDE
- PEG-75 LANOLIN
- GLYCERIN
- CITRIC ACID MONOHYDRATE
- FD&C RED NO. 4
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 42355-265 | 42355-265-05, 42355-265-14, 42355-265-19 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) | L605B5892V | IACT |
| DISODIUM COCOAMPHODIPROPIONATE | 6K8PRP397M | IACT |
| LAURAMINE OXIDE | 4F6FC4MI8W | IACT |
| PEG-75 LANOLIN | 09179OX7TB | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| FD&C RED NO. 4 | X3W0AM1JLX | 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 |
|---|---|---|---|---|---|---|
| 2cdca9e5-4332-e674-e063-6394a90aae08 | f97cf4d9-a402-4a43-aaab-b097b9d96124 | 2025-01-29 | Warnings | f97cf4d9-a402-4a43-aaab-b097b9d96124 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.