After Bite Natural

Manufacturer: Adventure Ready Brands
Effective date: 2023-01-19
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:53:22

Label at a glance#

ProductAfter Bite Natural

Active ingredientOATMEAL, CAMPHOR (NATURAL)

Label structure8 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 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#

Drug Facts

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Collodial Oatmeal (10%)

Camphor (1%)

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Topical Analgesic

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 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

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 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

Beeswax, Olive Oil, Peppermint.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Jar - LidJar - Back PanelBox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2597527	camphor 1 % / colloidal oatmeal 10 % Topical Ointment	PSN	2
2597527	camphor 0.01 MG/MG / colloidal oatmeal 0.1 MG/MG Topical Ointment	SCD	2
2597527	camphor 1 % / colloidal oatmeal 10 % Topical Ointment	SY	2

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
OATMEAL Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20181113

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
44224-0166-0	2025-01-30	C162847	48780-1	2cef2736-b623-d83d-e063-dadaa90ab31f	After Bite Natural

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
44224-0166-0	After Bite Natural	1 in 1 BOX	SALVE	1		2
44224-0166-0	After Bite Natural	18 g in 1 JAR	SALVE	18		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
44224-0166	AFTER BITE NATURAL (OATMEAL, CAMPHOR (NATURAL)) SALVE [ADVENTURE READY BRANDS]	2	Legacy NDC, 2 package rows	20230120_cfd3f684-4e1f-9ce3-e053-2995a90a50ee.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

After Bite Natural
OATMEAL, CAMPHOR (NATURAL)
PEG-8 BEESWAX
OATMEAL
OLIVE OIL
PEPPERMINT OIL
CAMPHOR (NATURAL)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
44224-0166	44224-0166-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PEG-8 BEESWAX	3C1QUF1TIR	IACT
OATMEAL	8PI54V663Y	ACTIB
OLIVE OIL	6UYK2W1W1E	IACT
PEPPERMINT OIL	AV092KU4JH	IACT
CAMPHOR (NATURAL)	N20HL7Q941	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f2a30cca-7ee5-6d2d-e053-2a95a90ad511			cfd3f684-4e1f-9ce3-e053-2995a90a50ee	2023-01-19	Warnings	Exact identifier spl id: f2a30cca-7ee5-6d2d-e053-2a95a90ad511 spl set id: cfd3f684-4e1f-9ce3-e053-2995a90a50ee

Reported adverse events (FAERS/openFDA)#

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