SARNA- camphor and menthol lotion 
Crown Laboratories

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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Sarna Original

Active ingredients

Camphor 0.5%

Menthol 0.5%

Purpose

External analgesic

Uses

Warnings

For external use only

When using this product

  • avoid contact with the eyes

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days.

If pregnant or breast-feeding,

ask a health care professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 2 years of age and older:

Children under 2 years of age:

Other information

Inactive ingredients

carbomer homopolymer type C, cetyl alcohol, DMDM hydantoin, fragrance, glyceryl monostearate, isopropyl myristate, petrolatum, polyoxyl 8 stearate, polyoxyl 100 stearate, purified water, sodium hydroxide, stearic acid

Questions or comments?

Call 1-833-279-6522

Principal Display Panel

#1 DERMATOLOGIST RECOMMENDED TOPICAL ANTI-ITCH BRAND

NDC 0316-0229-75

Steroid-Free

Sarna ORIGINAL

Camphor 0.5%, Menthol 0.5%

EXTERNAL ANALGESIC LOTION

ITCH RELIEF

Cools and soothes itch associated with:

Insect Bites

Poison Ivy

Sunburn

Soothes irritated skin


Net wt. 7.5 fl oz (222 mL)

Sarna is registered trademark of Crown Laboratories, Inc.

Distributed by: Crown Laboratories, Inc., Johnson City, TN 37604

©2019 Crown Laboratories, Inc.

p1170601

SARNA 
camphor and menthol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-0229
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)5 mg  in 1 mL
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
PETROLATUM (UNII: 4T6H12BN9U)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
POLYOXYL 8 STEARATE (UNII: 2P9L47VI5E)  
POLYOXYL 100 STEARATE (UNII: YD01N1999R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-0229-75222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/22/2011
Labeler - Crown Laboratories (079035945)
Establishment
NameAddressID/FEIBusiness Operations
Crown Laboratories, Inc.079035945manufacture(0316-0229)

Revised: 9/2021
Document Id: ccfc6e1c-b9e0-326e-e053-2a95a90a09fb
Set id: 7b2ff573-ca5a-d69a-e053-2a91aa0abcec
Version: 16
Effective Time: 20210927
 
Crown Laboratories