POST TREATMENT BALM- hydrocortisone cream 
Allure Labs 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.

----------

Drug Facts

Active Ingredient: Hydrocortisone 1%

Purpose: Anti-itch

Uses:

Warnings:

Do not use - If rashes appear on skin.

When using this Product:

Stop use and ask a doctor - If conditions worsens.

Keep out of reach of children:

Directions:

Inactive Ingredients:

Petrolatum, Carthamus Tinctorius (Safflower) Seed Oil, Tocopheryl Acetate, Zinc Oxide , Titanium Dioxide, Caprylic/Capric Triglyceride, Glyceryl Isostearate, Polyhydroxystearic Acid , Glycosaminoglycans, Dimethicone, Triethoxycaprylylsilane, PEG-8 , Tocopherol , Ascorbyl Palmitate , Ascorbic Acid, Citric Acid

Manufactured for DermaQuest®, Inc.

Hayward, CA 94544

1272 GK, NL Made in USA

dermaquestinc.com

IMGDQIPTB1oz

Manufactured for

DermaQuest®, Inc.

Hayward, CA-94544

1272 GK, NL Made in USA

dermaquestinc.com

IMGDQIPTB2oz

POST TREATMENT BALM 
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4077
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
GAG (UNII: U5T7CTT5KM)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SAFFLOWER (UNII: 4VBL71TY4Y)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ACETATE ION (UNII: 569DQM74SC)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
TOCOPHEROL (UNII: R0ZB2556P8)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
PETROLATUM (UNII: 4T6H12BN9U)  
SAFFLOWER OIL (UNII: 65UEH262IS)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62742-4077-229.6 g in 1 TUBE; Type 0: Not a Combination Product05/12/2015
2NDC:62742-4077-156.7 g in 1 TUBE; Type 0: Not a Combination Product05/12/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/12/2015
Labeler - Allure Labs Inc. (926831603)
Registrant - Allure Labs (926831603)
Establishment
NameAddressID/FEIBusiness Operations
Allure Labs926831603manufacture(62742-4077)

Revised: 12/2020
Document Id: b59a1b15-6485-5a52-e053-2a95a90a9614
Set id: faa803e6-453c-4d86-85dd-5a5dcdd72d02
Version: 2
Effective Time: 20201203
 
Allure Labs Inc.