Green Guard Maximum Strength Hydrocortisone Cream 1%

Drug Facts

Active ingredient

Hydrocortisone 1.0%

Purpose

Anti itch

Uses

for the temporary relief of itching associated with minor skin irritations, inflammation and rashes
for external genital, feminine and anal itching
other uses of this product should be only under the advice and supervision of a doctor

Warnings

For external use only

Do not use

Stop use and ask a doctor if

condition worsens or lasts more than 7 days, or clears and occurs again within a few days
you begin use of any other Hydrocortisone product unless you have consulted a doctor
bleeding occurs

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

for adults and children (2 years of age and older): apply to affected area 3 to 4 times daily
children under 12 years of age: for external anal itching, consult a doctor
children under 2 years of age: do not use, consult a doctor
adults for external anal itching when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly or by patting or blotting with an appropriate cleansing pad
gently dry by patting or botting with toilet tissue or a soft cloth before application of this product

Other information

Questions or comments?

1-800-869-6970

Inactive ingredient

emulsifying wax, ethanoll, methylparaben, mineral oil, paraffin, petrolatum, propylparaben, purified water, white wax

Green Guard Hydrocortisone Label

Maximum Strength

Hydrocortisone
cream 1%

Temporary relief of itching associated with minor skin irritation, inflammation and rashes

Green Guard

Order # 3103

25 Per Box

Net Wt 0.9 g (1/32 oz) Packets

3103

HYDROCORTISONE
hydrocortisone cream

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	10 mg in 1 g

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47682-397-71	20 in 1 BOX	04/15/2013	07/01/2019
1		0.9 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC:47682-397-12	10 in 1 BOX	04/15/2013	07/01/2019
2		0.9 g in 1 PACKET; Type 0: Not a Combination Product
3	NDC:47682-397-73	25 in 1 BOX	06/06/2016
3	NDC:47682-397-99	0.9 g in 1 PACKET; Type 0: Not a Combination Product
4	NDC:47682-397-35	144 in 1 BAG	06/30/2017
4		0.9 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	04/15/2013

Labeler - Unifirst First Aid Corporation (832947092)