OTC - ACTIVE INGREDIENT SECTION
ETYL ALCOHOL 0.80%
All Day Skin Relief with Colloidal Oats
- Manufacturer
- Lantern Enterprises Ltd.
- Effective date
- 2016-05-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 9
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:26:57
Label at a glance#
ProductAll Day Skin Relief with Colloidal Oats
Active ingredientCETYL ALCOHOL
Label structure8 sections
Label contents#
Full prescribing information#
PURPOSE
Skin Protectant
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center immediately.
INDICATIONS & USAGE SECTION
INDICATION AND USAGE
Relieves dry, itchy skin and provides hydration.
DOSAGE & ADMINISTRATION SECTION
DIRECTIONS
Adults and children over two years of age. Apply up to 3-4 times a day.
Chilldren under two years of age, consult a physician.
WARNINGS SECTION
WARNING
- For external use only - hands
- Stop use and contact a doctor if condition worsens and does not improve in seven days.
- Avoid contact with eyes. In case of contact with eyes, flush thoroughly with water
INACTIVE INGREDIENTS
WATER
GLYCERIN
DISTEARYLDIMONIUM CHLORIDE
PETROLATUM
ISOPROPYL PALMITATE
AVENA SATIVA (OAT) KERNEL FLOUR
BENZYL ALCOHOL
AVENA SATIVA (OAT) KERNEL OIL
STEARETH-20
AVENA SATIVA (OAT) KERNEL EXTRACT
BUTYROSPERMUM PARKII (SHEA BUTTER)
SODIUM CHLORIDE
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50154-012-50 | 2021-10-31 | C162847 | 48780-1 | 9d75b9d0-6cca-f424-e053-dadaa90a57ce | 31e07369-e63e-439c-e054-00144ff88e88 |
| 50154-012-50 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-6cca-f424-e053-dadaa90a57ce | 31e07369-e63e-439c-e054-00144ff88e88 |
Products#
Every source-derived product name is available through these pages.
- All Day Skin Relief with Colloidal Oats
- CETYL ALCOHOL
- AVENA SATIVA FLOWERING TOP
- STEARETH-20 METHACRYLATE
- SODIUM CHLORIDE NA-22
- WATER
- .ALPHA.-(.ALPHA.-AMINOPROPYL)BENZYL ALCOHOL
- GLYCERIN
- DISTEARYLDIMONIUM CHLORIDE
- SHEA BUTTER
- PETROLATUM
- ISOPROPYL PALMITATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50154-012 | 50154-012-50 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CETYL ALCOHOL | 936JST6JCN | ACTIB |
| AVENA SATIVA FLOWERING TOP | MA9CQJ3F7F | IACT |
| STEARETH-20 METHACRYLATE | A268NZ57NB | IACT |
| SODIUM CHLORIDE NA-22 | VMP9781061 | IACT |
| WATER | 059QF0KO0R | IACT |
| .ALPHA.-(.ALPHA.-AMINOPROPYL)BENZYL ALCOHOL | S8TT5K3C8Y | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| DISTEARYLDIMONIUM CHLORIDE | OM9573ZX3X | IACT |
| SHEA BUTTER | K49155WL9Y | IACT |
| PETROLATUM | 4T6H12BN9U | IACT |
| ISOPROPYL PALMITATE | 8CRQ2TH63M | 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 |
|---|---|---|---|---|---|---|
| cf6019e6-310d-47a4-e053-2995a90ab8c7 | 31e07369-e63e-439c-e054-00144ff88e88 | 2021-10-27 | Warnings | 31e07369-e63e-439c-e054-00144ff88e88 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.