QUALITY CHOICE ANTI-ITCH- hydrocortisone cream 
United Exchange Corp.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 Anti-itch Cream with Aloe 1oz 99259 ZDP (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

aloe vera leaf, aluminum sulfate octadecahydrate, calcium acetate, monohydrate, cetostearyl alcohol, dextrin, light mineral oil, maltodextrin, methylparaben, petrolatum, propylene glycol, propylparaben, purified water, sodium cetearyl sulfate, sodium lauryl sulfate, white wax

Distributed by: C.D.M.A., Inc.

43157 W 9 Mile Rd

Novi, MI 48375

www.qualitychoice.com

Made in China

99259

QUALITY CHOICE ANTI-ITCH 
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-693
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
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PETROLATUM (UNII: 4T6H12BN9U)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
WHITE WAX (UNII: 7G1J5DA97F)  
ICODEXTRIN (UNII: 2NX48Z0A9G)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ALUMINIUM SULFATE OCTADECAHYDRATE (UNII: TCS9L00G8F)  
CALCIUM ACETATE MONOHYDRATE (UNII: 7ZA48GIM5H)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-693-281 in 1 CARTON07/10/2019
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 finalpart34807/10/2019
Labeler - United Exchange Corp.Chain Drug Marketing Association Inc. (011920774)

Revised: 12/2019
Document Id: 995ffff7-8a98-656d-e053-2995a90a219f
Set id: 8fb76ccc-4638-e022-e053-2a95a90a7e03
Version: 2
Effective Time: 20191210
 
United Exchange Corp.Chain Drug Marketing Association Inc.