Dosage and administration
Directions - pump as needed into your palms and thoroughly spread on both hands - rub into skin until dry.
Pharmacys Prescription Hand Sanitizer
- Manufacturer
- Mission Series Inc. dba Prestige Beauty Care
- Effective date
- 2020-05-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:11:29
Label at a glance#
ProductPharmacys Prescription Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections
Label contents#
Full prescribing information#
Active Ingredients
Active ingredents - Ethyl Alcohol 62%
Purpose
Purpose - Antiseptic
Indications & Usage
Uses - Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.
Warnings
Warnings - For external use only.
Do not ingest or swallow.
Flammable. Keep away from fire or flame.
Do not apply around eyes. Do not use in ears & mouth.
When using this product
When using this product, avoid contact with eyes.
In case of contact, flush eyes with water.
Stop use
Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.
Keep out of reach of children
Keep out of reach of children. Do not use on children less than 2 months of age. Supervise use in children under 6 years of age to prevent accidental swallowing. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions - pump as needed into your palms and thoroughly spread on both hands - rub into skin until dry.
Other information
Other information - store at 20°C (68° to 77° F).
-may discolor fabrics.
Inactive Ingredients
Inactive ingredients: Water, Carbomer, Aminomethyl Propanol, Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Fragrance.
Distributed by:
Distributed by:
PRESTIGE BEAUTY CARE
1585 West Mission Blvd.
Pomona, CA 91766
Made in China
Pharmacys Prescription Hand Sanitizer
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73597-007-08 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-c06f-a426-e053-dadaa90af4c2 | Pharmacys Prescription Hand Sanitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73597-007-08 | Pharmacys Prescription Hand Sanitizer | 236.5 mL in 1 BOTTLE, PUMP | GEL | 236.5 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Pharmacys Prescription Hand Sanitizer
- Alcohol
- WATER
- AMINOMETHYLPROPANOL
- PROPYLENE GLYCOL
- .ALPHA.-TOCOPHEROL ACETATE
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
- GLYCERIN
- ALOE VERA LEAF
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73597-007 | 73597-007-08 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE | 0A5MM307FC | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | 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 |
|---|---|---|---|---|---|---|
| a5a3ee7b-3944-7589-e053-2995a90af1cb | a3d649ab-62b9-345f-e053-2a95a90a15ff | 2020-05-14 | Warnings | a5a3ee7b-3944-7589-e053-2995a90af1cb a3d649ab-62b9-345f-e053-2a95a90a15ff |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.