Dosage and administration
Place enough product on hands to cover all surfaces. Rub hands together until dry No rinsing required. No towels needed
Hand Sanitizer Gel
- Manufacturer
- AgroChem inc
- Effective date
- 2020-04-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:05:09
Label at a glance#
ProductHand Sanitizer Gel
Active ingredientALCOHOL
Label structure12 sections
Storage and handling
Do not store above 110°F (43°C) May discolor certain fabrics or surfaces
Label contents#
Full prescribing information#
Active Ingredient(s)
Ethyl alcohol 70% v/v. Purpose: Antiseptic
Purpose
Antimicrobial
Use
Hand sanitizer to help reduce bacteria on the skin that could cause disease Recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from heat or flame
OTC - WHEN USING SECTION
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Place enough product on hands to cover all surfaces. Rub hands together until dry
No rinsing required. No towels needed
Other information
- Do not store above 110°F (43°C) May discolor certain fabrics or surfaces
Inactive ingredients
Water (Aqua), Aloe Vera, Propylene Glycol, Carboxethyl Acrylate Crosspolymer, FD&C Blue #1, FD&C Yellow #5
DESCRIPTION SECTION
Hand Sanitizer Gel
Moisturizing with Aloe
Effective at eliminating more than 99.9% of many common harmful germs & bacteria in as little as 15 seconds.
Package Label - Principal Display Panel
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 17307-1114-1 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-88c1-a426-e053-dadaa90af4c2 | a28d4770-60ab-2963-e053-2995a90a641f |
| 17307-1114-2 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-88c1-a426-e053-dadaa90af4c2 | a28d4770-60ab-2963-e053-2995a90a641f |
| 17307-1114-3 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-88c1-a426-e053-dadaa90af4c2 | a28d4770-60ab-2963-e053-2995a90a641f |
| 17307-1114-4 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-88c1-a426-e053-dadaa90af4c2 | a28d4770-60ab-2963-e053-2995a90a641f |
| 17307-1114-5 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-88c1-a426-e053-dadaa90af4c2 | a28d4770-60ab-2963-e053-2995a90a641f |
| 17307-1114-6 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-88c1-a426-e053-dadaa90af4c2 | a28d4770-60ab-2963-e053-2995a90a641f |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17307-1114-1 | Hand Sanitizer Gel | 470 mL in 1 CONTAINER | SOLUTION | 470 | 1 | |
| 17307-1114-2 | Hand Sanitizer Gel | 940 mL in 1 BOTTLE, PUMP | SOLUTION | 940 | 1 | |
| 17307-1114-3 | Hand Sanitizer Gel | 3780 mL in 1 JUG | SOLUTION | 3780 | 1 | |
| 17307-1114-4 | Hand Sanitizer Gel | 18927 mL in 1 CONTAINER | SOLUTION | 18927 | 1 | |
| 17307-1114-5 | Hand Sanitizer Gel | 56781 mL in 1 DRUM | SOLUTION | 56781 | 1 | |
| 17307-1114-6 | Hand Sanitizer Gel | 208198 mL in 1 DRUM | SOLUTION | 208198 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17307-1114 | HAND SANITIZER GEL (ALCOHOL) SOLUTION [AGROCHEM INC] | 1 | Legacy NDC, 6 package rows | 20200407_a28d4770-60ab-2963-e053-2995a90a641f.zip |
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer Gel
- ALCOHOL
- PROPYLENE GLYCOL
- FD&C YELLOW NO. 5
- FD&C BLUE NO. 1
- AMMONIUM ACRYLOYLDIMETHYLTAURATE
- ALOE VERA LEAF
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 17307-1114 | 17307-1114-1, 17307-1114-2, 17307-1114-3, 17307-1114-4, 17307-1114-5, 17307-1114-6 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| FD&C YELLOW NO. 5 | I753WB2F1M | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| AMMONIUM ACRYLOYLDIMETHYLTAURATE | KBC00G95HI | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | 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 |
|---|---|---|---|---|---|---|
| a28d2478-ae5c-0c2b-e053-2a95a90aa614 | a28d4770-60ab-2963-e053-2995a90a641f | 2020-04-05 | Warnings | a28d2478-ae5c-0c2b-e053-2a95a90aa614 a28d4770-60ab-2963-e053-2995a90a641f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.