After Bite Advanced

Manufacturer
Tender Corporation d/b/a Adventure Ready Brands
Effective date
2025-12-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:26:45

Label at a glance#

ProductAfter Bite Advanced
Active ingredientSODIUM BICARBONATE
Label structure12 sections

Indications and uses

Temproarily protects and helps relieve minor skin irritation and itching due to insect bite poison ivy, oak sumac

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient / Purpose

OTC - ACTIVE INGREDIENT SECTION

Sodium Bicarbonate (Baking Soda) 5% Skin Protectant

Uses

INDICATIONS & USAGE SECTION

Temproarily protects and helps relieve minor skin irritation and itching due to insect bite poison ivy, oak sumac

Warnings

WARNINGS SECTION

For external use only.

if in eyes

WARNINGS AND PRECAUTIONS SECTION

flush with water for 15 minutes call a doctor

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

condition worsens , symptoms last more than 7 days or clear up and oiccur again within a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swollowed, get medical help or contact poisin control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Children under 2 years as a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ammonia, glycerin, purified water

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Box artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front of package Primary PackagingPrimary Packaging

Primary label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Primary PackagingPrimary PackagingLabel on actual product

3 Vial Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Secondary PackagingSecondary Packaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1547234sodium bicarbonate 5 % Topical SolutionPSN4
1547234sodium bicarbonate 50 MG/ML Topical SolutionSCD4
1547234NaHCO3 50 MG/ML Topical SolutionSY4
1547234sodium bicarbonate 5 % Topical SolutionSY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BICARBONATE ION Pharmacologic Class Indexing1Indexing - Pharmacologic Class20220121

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130044224610300GTIN-13: 0044224610300
EAN-13: 0044224610300
GTIN-12: 044224610300
UPC-A: 044224610300
GTIN storage (14 digits): 00044224610300
Box After Bite Advanced USA .jpg
Data codeITF00000000Box After Bite Advanced USA .jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44224-1103-0After Bite Advanced1 g in 1 VIALLIQUID14
44224-1103-2After Bite Advanced1 in 1 BOXLIQUID14
44224-1103-3After Bite Advanced14 g in 1 VIALLIQUID144
44224-1103-3After Bite Advanced3 in 1 BOXLIQUID34

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44224-110344224-1103-0, 44224-1103-2, 44224-1103-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32025-11-14monthly-update2026-06-03 17:40:03

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
After Bite AdvancedSODIUM BICARBONATETender Corporation d/b/a Adventure Ready Brands223d1de8-7940-bbdc-e063-6294a90a51d82025-12-18WarningsExact identifier
ndc (package): 44224-1103-2
ndc (package): 44224-1103-0
ndc (package): 44224-1103-3
ndc (product): 44224-1103
ndc11 (package): 44224110302
ndc11 (package): 44224110303
ndc11 (package): 44224110300
spl id: 4640051b-84fe-66c7-e063-6294a90a552e
spl set id: 223d1de8-7940-bbdc-e063-6294a90a51d8

Reported adverse events (FAERS/openFDA)#

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