QUALITY CHOICE ANTI ITCH- 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 Anti-Itch Cream Intensive Healing 1 oz. 99198 ZDP

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

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, .alpha.-tocopherol acetate, benzyl alcohol, cetyl alcohol, dimethicone 350, edetate disodium, gelatin hydrolysate, glycerin, glyceryl stearate/peg-100 stearate, magnesium ascorbyl, phosphate, matricaria chamomilla, flowering top, menthyl lactate,methyl gluceth-20, methylparaben, petrolatum,polysorbate 60, propylene glycol, propylparaben, purified water, steareth-2, steareth-21, stearyl alcohol, vitamin a palmitate

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

43157 W 9 Mile Rd.

Novi, MI 48375

www.qualitychoice.com

Made in China

99198

QUALITY CHOICE ANTI ITCH 
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-955
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
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PETROLATUM (UNII: 4T6H12BN9U)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
GLYCERIN (UNII: PDC6A3C0OX)  
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)  
STEARETH-21 (UNII: 53J3F32P58)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)  
MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02)  
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
DIMETHICONE 350 (UNII: 2Y53S6ATLU)  
GELATIN HYDROLYSATE (PORCINE SKIN, MW 3000) (UNII: 0K9R94573C)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
STEARETH-2 (UNII: V56DFE46J5)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-955-281 in 1 CARTON12/10/2019
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 finalpart34811/07/2019
Labeler - Chain Drug Marketing Association Inc (011920774)

Revised: 9/2022
Document Id: e936ddab-48d4-81b3-e053-2a95a90a54cd
Set id: 995fffc0-31ff-0810-e053-2995a90ae276
Version: 4
Effective Time: 20220921
 
Chain Drug Marketing Association Inc