DERMARAD RELIEF POST RADIATION CALMING- lidocaine 3 percent liquid 
Renu Laboratories, 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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DermaRad Relief Post Radiation Calming Serum with 3% Lidocaine

Active Ingredient

Lidocaine 3%

Purpose

External Analgesic

Uses

Temporarily relieves pain and itching due to

Warnings

For external use only

Stop use and ask a doctor if

Keep out of reach of children

If swallowed - get medical help or contact a poison control center right away

Directions

Inactive Ingredients:

Cyclopentasiloxane, Dihydroeugenol, Dimethicone, Dimethiconol, Dimethicone/Vinyl Dimethicone Crosspolymer, Helianthus Annuus (Sunflower) Seed Oil, Isoeugenyl Acetate, Petrolatum, Simmondsia Chinensis (Jojoba) Seed Oil, Squalane.

Manufactured in the U.S.A. for Dermamedics, LLC

Oklahoma City, OK 73112

www.dermamedics.com

1 800 990 6552

DERMAMEDICS

Post Radiation

Calming

Serum with

3 % Lidocaine

When using this product

Do not use in large quantities particularly over raw surfaces or blistered areas

Avoid contact with the eyes

PRODUCT BOX FOR POST RADIATION CALMING SERUM

product box

PRODUCT ARTWORK

PACKAGE ART

DERMARAD RELIEF POST RADIATION CALMING 
lidocaine 3 percent liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76348-970
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE1.5 g  in 50 mL
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
PETROLATUM (UNII: 4T6H12BN9U)  
JOJOBA OIL (UNII: 724GKU717M)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
ISOEUGENYL ACETATE (UNII: 9DF21GI8W6)  
SQUALANE (UNII: GW89575KF9)  
DIHYDROEUGENOL (UNII: A3XE712277)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76348-970-011 in 1 BOX08/08/2022
1NDC:76348-970-5050 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM01508/08/2022
Labeler - Renu Laboratories, Inc. (945739449)
Establishment
NameAddressID/FEIBusiness Operations
Renu Laboratories, Inc.945739449manufacture(76348-970)

Revised: 8/2022
Document Id: e5d6490d-34cf-19ac-e053-2995a90ab24b
Set id: e5d64929-fb9c-7ebc-e053-2995a90a9318
Version: 1
Effective Time: 20220808
 
Renu Laboratories, Inc.