Body
- Manufacturer
- Derma Glove | Mid Lab Incorporated
- Effective date
- 2016-09-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:23:04
Label at a glance#
ProductBody
Active ingredientALCOHOL
Label structure12 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Ethanol 62% v/v
OTC - PURPOSE SECTION
Antimicrobial
WARNINGS SECTION
For external use only. Flammable. Keep away from children.
OTC - WHEN USING SECTION
Do not use in or near eyes. In case of eye contact, rinse thoroughly with water.
OTC - STOP USE SECTION
If redness or irritation develop and persist for more than 72 hours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
If swallowed, get medical help or contact a Poison Control Center right away.
INDICATIONS & USAGE SECTION
Apply lotion directly onto body and rub with hands until dry. Product may be used on all skin surfaces. Children under 6 years of age should be supervised when using this product.
DOSAGE & ADMINISTRATION SECTION
Apply lotion directly onto body and rub with hands until dry. Product may be used on all skin surfaces. Children under 6 years of age should be supervised when using this product.
OTHER SAFETY INFORMATION
Do not store above 110oF (43oC). For additional information, see Safety Data Sheet (SDS).
INACTIVE INGREDIENT SECTION
Water (aqua), glycereth-18 (and) glycereth-18 ethylhexanoate, PEG 1450, PEG-10 dimethicone, cocamide MEA, ethylene glycol distearate, acrylate crosspolymer, fragrance (parfum), 2-amino-2-methyl-1-propanol, FD&C Blue #1.
OTC - QUESTIONS SECTION
Call 1-888-300-1225, Monday through Friday 8:00AM to 5:00PM EST/EDT.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70741-005-05 | 2023-07-31 | C162847 | 48780-1 | 9d75b9d0-4c7e-f424-e053-dadaa90a57ce | 83be6f41-16b5-4980-bee0-56ecafb94725 |
| 70741-005-05 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-4c7e-f424-e053-dadaa90a57ce | 83be6f41-16b5-4980-bee0-56ecafb94725 |
Products#
Every source-derived product name is available through these pages.
- Body
- Lotion
- ALCOHOL
- Water
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70741-005 | 70741-005-05 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| Water | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| 781fb553-7c69-4ecb-bcee-069c67dc1883 | 83be6f41-16b5-4980-bee0-56ecafb94725 | 2023-07-29 | Warnings | 83be6f41-16b5-4980-bee0-56ecafb94725 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.