FDA.reportPublic FDA data

After Bite Kids

Manufacturer
Adventure Ready Brands
Effective date
2024-02-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:08:44

Label at a glance#

ProductAfter Bite Kids
Active ingredientSODIUM BICARBONATE
Label structure10 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

Use cap to puncture safety seal. Adults and children 2 years and older for use as a cream, apply 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

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition 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 flush with water for 15 minutes and call a doctor.

Directions

DOSAGE & ADMINISTRATION SECTION

Use cap to puncture safety seal.

  • Adults and children 2 years and older for use as a cream, apply 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

Aloe Vera, Dimethicone, Emulsifying Wax, Eucalyptus Oil, Oleth-3 Phosphate, Oleth-10 Phosphate, Purified Water, Sodium Hydroxide, Tea Tree Oil and Vitamin E Acetate

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1722238sodium bicarbonate 5 % Topical CreamPSN4
1722238sodium bicarbonate 50 MG/ML Topical CreamSCD4
1722238NaHCO3 50 MG/ML Topical CreamSY4
1722238sodium bicarbonate 5 % Topical CreamSY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
SODIUM CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
90107-1280-12023-02-22C16284748780-1d6a99b39-95ef-a426-e053-dadaa90af4c2After Bite Kids
90107-1280-12022-01-28C16284748780-1d6a99b39-95ef-a426-e053-dadaa90af4c2After Bite Kids

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90107-1280-1After Bite Kids1 in 1 BOXCREAM14
90107-1280-1After Bite Kids20 g in 1 TUBECREAM204

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90107-1280AFTER BITE KIDS (SODIUM BICARBONATE) CREAM [ADVENTURE READY BRANDS]4Legacy NDC, 2 package rows20240217_afd4c2b9-b80f-b43a-e053-2995a90ac923.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90107-128090107-1280-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
DIMETHICONE92RU3N3Y1OIACT
EUCALYPTUS OIL2R04ONI662IACT
OLETH-3 PHOSPHATE8Q0Z18J1VLIACT
OLETH-10 PHOSPHATEQ95361F4VSIACT
WATER059QF0KO0RIACT
SODIUM HYDROXIDE55X04QC32IIACT
TEA TREE OILVIF565UC2GIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
1184b07f-3a22-6c95-e063-6294a90a8045afd4c2b9-b80f-b43a-e053-2995a90ac9232024-02-16WarningsExact identifier
spl id: 1184b07f-3a22-6c95-e063-6294a90a8045
spl set id: afd4c2b9-b80f-b43a-e053-2995a90ac923

Reported adverse events (FAERS/openFDA)#

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