Principal Display Panel - 28.4 G Tube Carton

Principal Display Panel - 28.4 G Tube Carton
SPL v6
SPL
SPL Set ID 28854187-91fd-42d6-a156-67ad6cca8a73
Route
TOPICAL
Published
Effective Date 2019-11-22
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Identifiers & Packaging


Description

Drug Facts


Medication Information

Warnings and Precautions

For external use only

Indications and Usage

temporarily relieves pain and itching associated with: insect bites minor burns sunburn minor skin irritations minor cuts scrapes rashes due to poison ivy, poison oak, and poison sumac dries the oozing and weeping of poison ivy, poison oak, and poison sumac

Dosage and Administration

do not use more often than directed adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily children under 2 years of age: ask a doctor

Description

Drug Facts

Section 42229-5

Drug Facts

Section 44425-7

To open: unscrew cap, use pointed end of cap to puncture seal. store at room temperature see carton or tube crimp for lot number and expiration date

Section 50565-1

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9

condition worsens or does not improve within 7 days symptoms persist for more than 7 days or clear up and occur again within a few days

Section 50567-7

avoid contact with eyes

Section 50569-3

on chicken pox on measles

Section 50570-1

on large areas of the body with any other product containing diphenhydramine, even one taken by mouth

Section 51727-6

cetyl alcohol, glyceryl stearate, glyceryl stearate/PEG-100 stearate, methylparaben, propylene glycol, propylparaben and purified water

Section 51945-4

sunmark ® anti-itch cream 2% diphenhydramine hydrochloride Topical Analgesic/Antihistamine Skin Protectant EXTRA STRENGTH NET WT 1 OZ (28.4 g)

Section 53413-1

Call 1-866-923-4914

Section 55105-1

Active ingredients Purpose Diphenhydramine hydrochloride 2% Topical analgesic Zinc acetate 0.1% Skin protectant


Structured Label Content

Indications and Usage (34067-9)

temporarily relieves pain and itching associated with: insect bites minor burns sunburn minor skin irritations minor cuts scrapes rashes due to poison ivy, poison oak, and poison sumac dries the oozing and weeping of poison ivy, poison oak, and poison sumac

Dosage and Administration (34068-7)

do not use more often than directed adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily children under 2 years of age: ask a doctor

Warnings and Precautions (34071-1)

For external use only

Section 42229-5 (42229-5)

Drug Facts

Section 44425-7 (44425-7)

To open: unscrew cap, use pointed end of cap to puncture seal. store at room temperature see carton or tube crimp for lot number and expiration date

Section 50565-1 (50565-1)

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9 (50566-9)

condition worsens or does not improve within 7 days symptoms persist for more than 7 days or clear up and occur again within a few days

Section 50567-7 (50567-7)

avoid contact with eyes

Section 50569-3 (50569-3)

on chicken pox on measles

Section 50570-1 (50570-1)

on large areas of the body with any other product containing diphenhydramine, even one taken by mouth

Section 51727-6 (51727-6)

cetyl alcohol, glyceryl stearate, glyceryl stearate/PEG-100 stearate, methylparaben, propylene glycol, propylparaben and purified water

Section 51945-4 (51945-4)

sunmark ® anti-itch cream 2% diphenhydramine hydrochloride Topical Analgesic/Antihistamine Skin Protectant EXTRA STRENGTH NET WT 1 OZ (28.4 g)

Section 53413-1 (53413-1)

Call 1-866-923-4914

Section 55105-1 (55105-1)

Active ingredients Purpose Diphenhydramine hydrochloride 2% Topical analgesic Zinc acetate 0.1% Skin protectant


Raw Label Data

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