FDA.reportPublic FDA data

After Bite Advanced

Manufacturer
Adventure Ready Brands
Effective date
2021-01-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:55:25

Label at a glance#

ProductAfter Bite Advanced
Active ingredientSODIUM BICARBONATE
Label structure7 sections

Indications and uses

Temporarily protects and helps relieve minor skin irritation and itching due to Insect bites Poison ivy, oak, or sumac

Dosage and administration

Adults and children 2 years and older apply directly to the affected area of the skin as needed or as directed by a doctor Children under 2 years ask a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Bicarbonate (Baking Soda) 5%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

Temporarily protects and helps relieve minor skin irritation and itching due to

  • Insect bites
  • Poison ivy, oak, or sumac

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes
  • do not bandage or cover until dry

Stop use and ask a doctor If

OTC - STOP USE SECTION

  • conditions worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

If in eyes

SPL UNCLASSIFIED SECTION

flush with water for 15 minutes and call a doctor

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years and older apply directly to the affected area of the skin as needed or as directed by a doctor
  • Children under 2 years ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ammonia, Cyclohexasiloxane, Cyclopentasiloxane, Glycerin, Purified Water

After Bite

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90107-103090107-1030-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMMONIA5138Q19F1XIACT
CYCLOMETHICONE 6XHK3U310BAIACT
CYCLOMETHICONE 50THT5PCI0RIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
SODIUM BICARBONATE8MDF5V39QOACTIB

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b982b333-7ad6-c7a5-e053-2a95a90af3b0af99f49e-c06e-093c-e053-2a95a90a78212021-01-22WarningsExact identifier
spl id: b982b333-7ad6-c7a5-e053-2a95a90af3b0
spl set id: af99f49e-c06e-093c-e053-2a95a90a7821

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.