Indications and uses
hand sanitizer to help reduce bacteria on the skin
PREMIER PURE Protection
- Manufacturer
- RPP PRODUCTS, INC.
- Effective date
- 2020-04-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:05:55
Label at a glance#
ProductPREMIER PURE Protection
Active ingredientALCOHOL
Label structure8 sections
Dosage and administration
Put enough product in your palm to cover hands and rub hands together briskly until dry. children under 6 years of age should be supervised when using this PREMIER PURE
Label contents#
Full prescribing information#
Active ingredient
Ethyl Alcohol 80% v/v
Purpose
Antimicrobial
Uses
hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable, keep away from fire or flame
For external use only
When using this product do not use in or near the eyes
In case of contact rinse thoroughly with water
When using this product
do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask doctor if
irritation or rash appears and lasts
Keep out of reach of children.
If swallowed, get medical help right away or contact a Poison Control Center immediately.
Directions
- Put enough product in your palm to cover hands and rub hands together briskly until dry.
- children under 6 years of age should be supervised when using this PREMIER PURE
Other information
- Store below 1100 F (430C)
- May discolor certain fabrics or surfaces
- This product does not contain any chemicals known to the State of California to cause cancer, birth defects, or any other reproductive harm
Inactive ingredients
Water, Glycerin, Propylene Glycol, Triisopropanolamine, Carbomer, Fragrance
Product Label
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73945-003-01 | PREMIER PURE Protection | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | 1 | |
| 73945-003-02 | PREMIER PURE Protection | 88.72 mL in 1 BOTTLE, PLASTIC | LIQUID | 88.72 | 1 | |
| 73945-003-03 | PREMIER PURE Protection | 118.3 mL in 1 BOTTLE, PLASTIC | LIQUID | 118.3 | 1 | |
| 73945-003-04 | PREMIER PURE Protection | 236.59 mL in 1 BOTTLE, PLASTIC | LIQUID | 236.59 | 1 | |
| 73945-003-05 | PREMIER PURE Protection | 295.74 mL in 1 BOTTLE, PLASTIC | LIQUID | 295.74 | 1 | |
| 73945-003-06 | PREMIER PURE Protection | 443.60 mL in 1 BOTTLE, PLASTIC | LIQUID | 443.60 | 1 | |
| 73945-003-07 | PREMIER PURE Protection | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | 1 | |
| 73945-003-08 | PREMIER PURE Protection | 946 mL in 1 BOTTLE, PLASTIC | LIQUID | 946 | 1 | |
| 73945-003-09 | PREMIER PURE Protection | 1890 mL in 1 BOTTLE, PLASTIC | LIQUID | 1890 | 1 | |
| 73945-003-10 | PREMIER PURE Protection | 2000 mL in 1 BOTTLE, PLASTIC | LIQUID | 2000 | 1 | |
| 73945-003-11 | PREMIER PURE Protection | 2800 mL in 1 BOTTLE, PLASTIC | LIQUID | 2800 | 1 | |
| 73945-003-12 | PREMIER PURE Protection | 3780 mL in 1 BOTTLE, PLASTIC | LIQUID | 3780 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- PREMIER PURE Protection
- Ethyl Alcohol
- ALCOHOL
- WATER
- GLYCERIN
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
- TRIISOPROPANOLAMINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73945-003 | 73945-003-01, 73945-003-02, 73945-003-03, 73945-003-04, 73945-003-05, 73945-003-06, 73945-003-07, 73945-003-08, 73945-003-09, 73945-003-10, 73945-003-11, 73945-003-12 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) | 4Q93RCW27E | IACT |
| TRIISOPROPANOLAMINE | W9EN9DLM98 | 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 |
|---|---|---|---|---|---|---|
| 72c9b620-850c-4f2b-8a5e-a4c2b9b51db2 | 2e2b3a15-4caa-42a1-a5ae-61ca4d941713 | 2020-04-10 | Warnings | 72c9b620-850c-4f2b-8a5e-a4c2b9b51db2 2e2b3a15-4caa-42a1-a5ae-61ca4d941713 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.