QUALITY CHOICE ITCH RELIEF- hydrocortisone cream 
Chain Drug Marketing Association Inc.

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.

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QC 1% Hydrocortisone Cream Max. Strength 1 oz 99260 (2019)

Active ingredient Purpose

Hydrocortisone 1%..................................................Anti-itch

Uses

Warnings

For external use only

Do not use

When using this product

Stop use and ask a doctor

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Other information

Inactive ingredients

butylated hydroxytoluene, cetostearyl alcohol, light mineral oil, methylparaben, propylene glycol, propylparaben, purified water, sorbitan monooleate, steareth-20, stearic acid

Distributed by:

C.D.M.A., Inc.

43157 W 9 Mile Rd

Novi, MI 48375

www.qualitychoice.com

Made in China

99260

QUALITY CHOICE ITCH RELIEF 
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-603
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
STEARETH-20 (UNII: L0Q8IK9E08)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-603-281 in 1 CARTON07/15/2019
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/15/2019
Labeler - Chain Drug Marketing Association Inc. (011920774)

Revised: 12/2019
Document Id: 995ff746-62b1-cdbc-e053-2a95a90a5411
Set id: 8dc1ac1e-de7f-44e1-e053-2a95a90a182e
Version: 2
Effective Time: 20191210
 
Chain Drug Marketing Association Inc.