Indications and uses
For Personal hand hygiene to help the spread of bacteria. Can be used in place of hand washing if soap and water are not available.
Moxie
- Manufacturer
- Apollo Health and Beauty Care
- Effective date
- 2021-03-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:38:51
Label at a glance#
ProductMoxie
Active ingredientALCOHOL
Label structure8 sections
Dosage and administration
For occasional and personal use Rub thoroughly into hands for at least 30 seconds. Allow to dry Children under 6 years should be supervised when using this product
Storage and handling
Store at a temperature below 110 0 F (43 0 C) May discolor certain fabrics or surfaces
Label contents#
Full prescribing information#
Active Ingredients
Ethyl Alcohol (70%)
Purpose
Antiseptic
Uses
For Personal hand hygiene to help the spread of bacteria. Can be used in place of hand washing if soap and water are not available.
Warnings
- For External use only
- Flammable
- Keep away from source of heat or fire.
When using this product
Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not Inhale.
Do not use
- on children less than 2 months of age
- on open skin wounds
- on broken or damaged skin
Stop use and ask a doctor
If Irritation or redness develops and lasts.
Keep out of reach of children
In case of accidental ingestion, get medical help or contact a Poison Control Centre immediately
Directions
- For occasional and personal use
- Rub thoroughly into hands for at least 30 seconds. Allow to dry
- Children under 6 years should be supervised when using this product
Other Information
- Store at a temperature below 1100F (430C)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Water (Aqua), PEG-6, AMP-Acrylates/Vinyl Isodecanate Crosspolymer, Isopropyl Myristate, Glycerin, Isopropyl Alcohol, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Yellow 5 (Cl19140), Blue 1 (Cl42090)
24 oz sanitizer
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63148-662-24 | 2024-01-30 | C162847 | 48780-1 | 1030e365-0f24-111a-e063-dadaa90a10e2 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63148-662-24 | Moxie | 710 mL in 1 BOTTLE, PLASTIC | GEL | 710 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Moxie
- Ethyl Alcohol
- ALCOHOL
- WATER
- POLYETHYLENE GLYCOL 300
- ISOPROPYL ALCOHOL
- GLYCERIN
- ISOPROPYL MYRISTATE
- ALOE VERA LEAF
- .ALPHA.-TOCOPHEROL ACETATE, DL-
- ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)
- BASIC YELLOW 5
- BASIC BLUE 1
- FRAGRANCE CUCUMBER ALOE ORC1802955
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63148-662 | 63148-662-24 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 22ded40a-107a-4a8a-bc50-b5fa2c958c7d | 82ddffa9-fc50-4194-9ffb-e48287ed3e15 | 2021-03-10 | Warnings | 22ded40a-107a-4a8a-bc50-b5fa2c958c7d 82ddffa9-fc50-4194-9ffb-e48287ed3e15 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.