FDA Label for Anti-itch
View Indications, Usage & Precautions
Anti-itch Product Label
The following document was submitted to the FDA by the labeler of this product Target Corporation. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Drug Fact
Active Ingredients
Diphenhydramine HCL 2%
Zinc Acetate 0.1%
Purpose
Topical analgesic
Skin protectant
Uses
For temporary relief from pain and itching associated with :
- insect bites
- minor burns
- sunburn
- minor skin irritations
- rashes due to poison ivy, poison oak, and poison sumac
- ivy
- oak
- sumac
Dries the oozing and weeping of poison
Warningsfor External Use Only
Do not use
- on large areas of the body
- with any other product containing diphenhydramine , even one taken by the mouth.
- on chicken pox
- on measles
- conditions worsen or does not improve within 7 days
- symptoms persist for more than 7 days or clear up and occur agian within a few days
Ask a Doctor before use
When using this product avoid contact with eyes.
Stop use and ask a doctor if
Directions
- do not use more than directed
- adults and children 2 years of age and older; apply to affected areas not more than 3 to 4 times daily
- children under 2 years of age , consult a doctor
Other Information
Store at controlled room temperature 20°-25°C (68° - 77°F)
Close the cap tightly after use
Inactive Ingredients
Cetyl Alcohol, Citric Acid, Diazolldinyl Urea, Glyceral Stearate, Methylparaben, Polyethylene Glycol Monsterate 1000, Sodium Citrate, Water
(Purified)
Questions Or Comments? 1-800-910-6874
Principal Display Panel
Target Up&Up NDC 11673-865-28
Extra Strength Itch Relief
Diphenhydramine HCL 2% / Zinc Aceate 0.1%
Anti-itch cream
NET WT 1 OZ (28g)
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