Dosage and administration
wet hands thoroughly with product and allow to dry without wiping
NERF Hand Sanitizer
- Manufacturer
- Gold Orient International Limited
- Effective date
- 2020-07-23
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:22:26
Label at a glance#
ProductNERF Hand Sanitizer (NRF 100)
Active ingredientALCOHOL
Label structure12 sections
Storage and handling
Store between 66 to 77F (20-25C) Do not store above 110F (43C) You may report a serious adverse reaction to this product to Report Reaction, LLC, PO Box 22 Plainsboro, NJ 08536
Label contents#
Full prescribing information#
Active Ingredient(s)
Alcohol 62% v/v.
Purpose
Antiseptic
Use
For hand-washing to decrease bacteria on the skin, only when water is not available
Warnings
For external use only. Flammable. Keep away from heat or flame
Do not use
- in children less than 2 months of age
- on open skin wounds
OTC - WHEN USING SECTION
- Do not get into eyes.
- if contact occurs, rinse eyes thoroughly with water
OTC - STOP USE SECTION
irritation and redness develop
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
- wet hands thoroughly with product and allow to dry without wiping
Other information
- Store between 66 to 77F (20-25C)
- Do not store above 110F (43C)
- You may report a serious adverse reaction to this product to Report Reaction, LLC, PO Box 22 Plainsboro, NJ 08536
Inactive ingredients
Water, Glycerin, Acrylates/ C10-30 Alkyl Acrylates Crosspolymer, Fragrance, Polysorbate 20, Sodium Hydroxide, Yellow 5, Blue 1
Package Label - Principal Display Panel
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51522-030-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-dece-a426-e053-dadaa90af4c2 | Nerf (NRF 100) |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51522-030-01 | NERF Hand Sanitizer(NRF 100) | 30 mL in 1 BOTTLE, PLASTIC | GEL | 30 | 1 | |
| 51522-030-01 | NERF Hand Sanitizer(NRF 100) | 1 in 1 POUCH | GEL | 1 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- NERF Hand Sanitizer (NRF 100)
- ALCOHOL
- POLYSORBATE 20
- GLYCERIN
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
- WATER
- FD&C BLUE NO. 1
- SODIUM HYDROXIDE
- FD&C YELLOW NO. 5
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51522-030 | 51522-030-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POLYSORBATE 20 | 7T1F30V5YH | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) | 71DD5V995L | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| FD&C YELLOW NO. 5 | I753WB2F1M | 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 |
|---|---|---|---|---|---|---|
| ab1c8c03-28e3-f5ec-e053-2995a90a3321 | ab1c6f37-3b69-23fb-e053-2995a90a932f | 2020-07-23 | Warnings | ab1c8c03-28e3-f5ec-e053-2995a90a3321 ab1c6f37-3b69-23fb-e053-2995a90a932f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.