SARNA- camphor and menthol lotion 
Crown Laboratories

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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, PEG-8 stearate, PEG-100 stearate, purified water, sodium hydroxide, stearic acid

Questions or comments?

Call 1-833-279-6522

Principal Display Panel

NDC 0316-0229-75

#1 DERMATOLOGIST RECOMMENDED TOPICAL ANTI-ITCH BRAND

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

Net wt. 7.5 fl oz (222 mL)

P11706.01

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 Product12/01/201801/31/2026
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01702/22/201101/31/2026
Labeler - Crown Laboratories (079035945)
Establishment
NameAddressID/FEIBusiness Operations
Crown Laboratories, Inc.079035945manufacture(0316-0229)

Revised: 5/2024
Document Id: 19c50727-d349-b9f5-e063-6294a90aef89
Set id: 7b2ff573-ca5a-d69a-e053-2a91aa0abcec
Version: 19
Effective Time: 20240531
 
Crown Laboratories