AVON Skin So Soft Bug Guard Plus Anti-Itch - THE AVON COMPANY
- Manufacturer
- THE AVON COMPANY
- Effective date
- 2026-09-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- daily-update
- Hydrated at
- 2026-09-26 01:01:21
Label at a glance#
ProductAVON Skin So Soft Bug Guard Plus Anti-Itch
Active ingredientMENTHOL
Label structure7 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Menthol 0.5 %......
OTC - PURPOSE SECTION
Purpose
.........External Analgesic
INDICATIONS & USAGE SECTION
Uses
For the temporary relief of pain and/or itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites or minor skin irritations.
WARNINGS SECTION
Warnings
For external use only
OTC - WHEN USING SECTION
When using this product
- Avoid contact with eyes.
OTC - STOP USE SECTION
Stop use and ask a doctor if
- condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
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 right away
DOSAGE & ADMINISTRATION SECTION
Directions
Adults and children 2 years of age and older:
- Apply to affected area not more than 3 to 4 times daily
Children under 2 years of age:
- Consult a doctor
INACTIVE INGREDIENT SECTION
Inactive Ingredients:
Water/Eau, C12-15 Alkyl Benzoate, Ethylhexyl Palmitate, Glycerin, SD Alcohol 40-B, Butylene Glycol, Glyceryl Stearate, Ceteareth-20, Avena Sativa (Oat) Meal Extract, Citric Acid, Ceteareth-12, Cetearyl Alcohol, Cetyl Palmitate, Cholesterol, Chlorphenesin, Sodium Hydroxide, Sodium Dehydroacetate.
OTC - QUESTIONS SECTION
Questions?
Call
1-800-FOR-AVON
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- AVON Skin So Soft Bug Guard Plus Anti-Itch
- menthol
- WATER
- C12-15 ALKYL BENZOATE
- ETHYLHEXYL PALMITATE
- GLYCERIN
- DEHYDRATED ALCOHOL
- BUTYLENE GLYCOL
- GLYCERYL STEARATE
- CETEARETH-20
- OATMEAL
- CITRIC ACID
- CETEARETH-12
- CETEARYL ALCOHOL
- CETYL PALMITATE
- CHOLESTEROL
- CHLORPHENESIN
- SODIUM HYDROXIDE
- SODIUM DEHYDROACETATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10096-0382 | 10096-0382-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL | L7T10EIP3A | ACTIB |
| WATER | 059QF0KO0R | IACT |
| C12-15 ALKYL BENZOATE | A9EJ3J61HQ | IACT |
| ETHYLHEXYL PALMITATE | 2865993309 | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| DEHYDRATED ALCOHOL | 3K9958V90M | IACT |
| BUTYLENE GLYCOL | 3XUS85K0RA | IACT |
| GLYCERYL STEARATE | 230OU9XXE4 | IACT |
| CETEARETH-20 | YRC528SWUY | IACT |
| OATMEAL | 8PI54V663Y | IACT |
| CITRIC ACID | 2968PHW8QP | IACT |
| CETEARETH-12 | 7V4MR24V5P | IACT |
| CETEARYL ALCOHOL | 2DMT128M1S | IACT |
| CETYL PALMITATE | 5ZA2S6B08X | IACT |
| CHOLESTEROL | 97C5T2UQ7J | IACT |
| CHLORPHENESIN | I670DAL4SZ | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| SODIUM DEHYDROACETATE | 8W46YN971G | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.