Drug Facts Box OTC-Active Ingredient Section
Chloroxylenol 0.3%
High Five Antiseptic Hand and Body Wash
- Manufacturer
- Jani-Source, LLC | ABC Compounding Co., Inc.
- Effective date
- 2019-01-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:34:20
Label at a glance#
ProductHigh Five Antiseptic Hand and Body Wash
Active ingredientCHLOROXYLENOL
Label structure10 sections
Label contents#
Full prescribing information#
Drug Facts Box OTC-Purpose Section
Antiseptic
Drug Facts Box OTC-Indications & Usage Section
for hand-washing to decrease bacteria on the skin
Drug Facts Box OTC-Warnings Section
For external use only
Drug Facts Box OTC-When Using Section
do not get into eyes
if contact occurs, rinse eyes thoroughly with water
Drug Facts Box OTC-Stop Use Section
irritation and redness develop
Drug Facts Box OTC-Keep Out of Reach of Children Section
if swallowed, get medical help or contact a Poison Control Center right away
Drug Facts Box OTC-Dosage & Administration Section
- wet hands and forearms
- apply 5 milliliters (teaspoonful) or palmful to hands and forearms
- scrub thoroughly for 1 minute and rinse
Drug Facts Box OTC-Inactive Ingredient Section
water, decyl glucoside, sodium laureth sulfate, cocamide MIPA, propylene glycol, sodium chloride, DMDM hydantoin, methylchloroisothiazolinone, methylisothiazolinoe, fragrance, aloe barbadensis, acid red 1
High Five Antiseptic Hand and Body Wash 6875
High Five Antiseptic Hand and Body Wash
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- High Five Antiseptic Hand and Body Wash
- CHLOROXYLENOL
- WATER
- PROPYLENE GLYCOL
- SODIUM LAURETH SULFATE
- DECYL GLUCOSIDE
- SODIUM CHLORIDE
- METHYLCHLOROISOTHIAZOLINONE
- METHYLISOTHIAZOLINONE
- ACID RED 1
- DMDM HYDANTOIN
- ALOE VERA LEAF
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49557-875 | 49557-875-06, 49557-875-17, 49557-875-24, 49557-875-01, 49557-875-03, 49557-875-05, 49557-875-07, 49557-875-09, 49557-875-10, 49557-875-11, 49557-875-12, 49557-875-13, 49557-875-14, 49557-875-15, 49557-875-28, 49557-875-27, 49557-875-55, 49557-875-08, 49557-875-16, 49557-875-18, 49557-875-19, 49557-875-20, 49557-875-35 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CHLOROXYLENOL | 0F32U78V2Q | ACTIB |
| WATER | 059QF0KO0R | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| SODIUM LAURETH SULFATE | BPV390UAP0 | IACT |
| DECYL GLUCOSIDE | Z17H97EA6Y | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| METHYLCHLOROISOTHIAZOLINONE | DEL7T5QRPN | IACT |
| METHYLISOTHIAZOLINONE | 229D0E1QFA | IACT |
| ACID RED 1 | 3365R6427R | IACT |
| DMDM HYDANTOIN | BYR0546TOW | 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 |
|---|---|---|---|---|---|---|
| fe183109-d940-27e8-e053-6294a90a453a | 98608778-4cf4-48a7-ac77-7c6247eb33a3 | 2023-06-14 | Warnings | 98608778-4cf4-48a7-ac77-7c6247eb33a3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.