Dosage and administration
apply to affected area not more than 3 to times daily. Children under 2 years,do not use;ask a doctor.
Insect Bite Relief Spray 51414-106
- Manufacturer
- Yuyao Jessie Commodity Co.,Ltd.
- Effective date
- 2022-12-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:44:06
Label at a glance#
ProductInsect Bite Relief
Active ingredientHYDROCORTISONE
Label structure6 sections
Label contents#
Full prescribing information#
Active Ingredient
Hydrocortisone 1%
Purpose
Anti-itch
Use
Temporarity relieves itching associated with minor skin irritations,inflammation and rashes due to :eczema,psoriasis ,insect bites,detergents,jewelry,cosmetics,soaps,seborrheic dermatitis and more
WARNINGS
For External use only.
Do not use in or near the eyes,for diaper rash ;ask a doctor.
ask a doctor before use if you are using any other hydrocortisone product.
stop use and ask a doctor,if .conditon worsens or if symptoms persist ofr more than 7 days. symptoms last more than 7 days or clear up and occur again within a few days.
keep out of reach of children
if product is swallowed,get medical help or contact a Poison Control Center right away.
Directions
apply to affected area not more than 3 to times daily.
Children under 2 years,do not use;ask a doctor.
Inactive ingredients
water,cetearyl alcohol,glycerin,ceteareth-20,isoproply myristate ,edta-2na,phenoxyethanol,tocopheryl acetate,aloe barbadensis leaf juice
lebel
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- Insect Bite Relief
- Hydrocortisone
- MENTHOL
- PROPYLENE GLYCOL
- ALCOHOL
- GLYCERIN
- WATER
- ALOE VERA LEAF
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51414-106 | 51414-106-01, 51414-106-02, 51414-106-03, 51414-106-04, 51414-106-06, 51414-106-07, 51414-106-08, 51414-106-09, 51414-106-05, 51414-106-10 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL | L7T10EIP3A | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| HYDROCORTISONE | WI4X0X7BPJ | ACTIB |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| f0033086-4ab1-b3e3-e053-2995a90ad171 | 62067592-a747-1cc4-e053-2a91aa0a6139 | 2022-12-17 | Warnings | f0033086-4ab1-b3e3-e053-2995a90ad171 62067592-a747-1cc4-e053-2a91aa0a6139 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.