Drug Facts Box OTC-Active Ingredient Section
benzalkonium chloride USP 0.13%
Insti-Foam Sanitizer
- Manufacturer
- Share Corporation | ABC Compounding Co., Inc.
- Effective date
- 2022-05-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:01:43
Label at a glance#
ProductInsti-Foam Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections
Label contents#
Full prescribing information#
Drug Facts Box OTC-Indications & Usage Section
For hand-washing to decrease bacteria on the skin, only when water is not available
Drug Facts Box OTC-Warnings Section
For external use only
Drug Facts Box OTC-Purpose Section
Antiseptic
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
press pump twice to deliver two squirts (about a quarter size) of foaming product onto the palm of your hand
rub hands together until dry
wash hands with soap and water at earliest opportunity
Drug Facts Box-OTC Inactive Ingredient Section
water, glycerine, dimethicone, DMDM hydantoin, iodopropynl butylcarbamate, methylchloroisothiazolinone, methylisothiazolinone, fragrance
Insti-Foam Hand Sanitizer
Insti-Foam Hand Sanitizer
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68654-086-14 | 2025-02-01 | C162847 | 48780-1 | 2cef2736-a9bf-d83d-e063-dadaa90ab31f | 6457 Insti-Foam Sanitizer Drug Facts and Label |
Products#
Every source-derived product name is available through these pages.
- Insti-Foam Sanitizer
- BENZALKONIUM CHLORIDE
- WATER
- GLYCERIN
- DIMETHICONE
- DMDM HYDANTOIN
- IODOPROPYNYL BUTYLCARBAMATE
- METHYLCHLOROISOTHIAZOLINONE
- METHYLISOTHIAZOLINONE
- BENZALKONIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 68654-086 | 68654-086-14 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| DIMETHICONE | 92RU3N3Y1O | IACT |
| DMDM HYDANTOIN | BYR0546TOW | IACT |
| IODOPROPYNYL BUTYLCARBAMATE | 603P14DHEB | IACT |
| METHYLCHLOROISOTHIAZOLINONE | DEL7T5QRPN | IACT |
| METHYLISOTHIAZOLINONE | 229D0E1QFA | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 2d014d0c-e814-c82a-e063-6394a90a8a51 | de1fed92-05d8-58a0-e053-2a95a90a0efc | 2025-01-31 | Warnings | de1fed92-05d8-58a0-e053-2a95a90a0efc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.