OTC Medication Information: After Bite Natural

AFTER BITE NATURAL- oatmeal and camphor (natural) salve
Adventure Ready Brands

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Drug Facts

Active Ingredient

Collodial Oatmeal (10%)

Camphor (1%)

Purpose

Skin Protectant

Topical Analgesic

Uses

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

  • insect bites
  • poison ivy, oak, or sumac

Warnings

For external use only

When using this product

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

Stop use and ask doctor if

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

Keep out of reach of children.

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

  • 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

Beeswax, Olive Oil, Peppermint.

Jar -- Lid
(click image for full-size original)
Jar -- Back Panel
(click image for full-size original)
Box
(click image for full-size original)

AFTER BITE NATURAL
oatmeal, camphor (natural) salve
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:44224-0166
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OATMEAL (OATMEAL) OATMEAL 100 mg in 1 g
CAMPHOR (NATURAL) (CAMPHOR (NATURAL)) CAMPHOR (NATURAL) 10 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
PEG-8 BEESWAX
OLIVE OIL
PEPPERMINT OIL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:44224-0166-0 1 JAR in 1 BOX contains a JAR
1 18 g in 1 JAR This package is contained within the BOX (44224-0166-0)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 04/01/2022
Labeler — Adventure Ready Brands (064437304)
Registrant — Adventure Ready Brands (064437304)
Establishment
Name Address ID/FEI Operations
Adventure Ready Brands 064437304 manufacture (44224-0166)

Revised: 01/2023 Adventure Ready Brands

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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