GOLD BOND MEDICATED CRACKED FOOT SKIN RELIEF- petrolatum ointment 
Chattem, Inc.

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Gold Bond Medicated Cracked Skin Relief Ointment

Gold Bond Medicated Cracked Foot Skin Relief

Skin Protectant Ointment Petrolatum 30%

Drug Facts

Active ingredient

Petrolatum 30%

Purpose

Skin protectant

Uses

■ temporarily protects minor: ■ cuts ■ scrapes ■ burns

■ temporarily protects and helps relieve chapped or cracked skin

■ helps protect from the drying effects of wind and cold weather

Warnings

For external use only

When using this product

■ avoid contact with eyes

Stop use and ask a doctor if

■ condition worsens ■ symptoms last more than 7 days or clear up and occur again within a few days

Do not use on

■ deep or puncture wounds ■ animal bites ■ serious burns

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately

Directions

■ apply as needed.

Inactive ingredients

water, glycerin, glyceryl stearate, dimethicone, steareth-21, distearyldimonium chloride, polyethylene, stearyl alcohol, cetearyl alcohol, behentrimonium methosulfate, hydrolyzed jojoba esters, jojoba esters, aloe barbadensis leaf juice, allantoin, butyrospermum parkii (shea) butter extract, ceramide NP, ceramide NS, ceramide EOS, ceramide EOP, ceramide AP, cocodimonium hydroxypropyl hydrolyzed rice protein, cetyl alcohol, biotin, cholesterol, caprooyl phytosphingosine, polysorbate 60, caprooyl sphingosine, bisabolol, 3-O-ethyl ascorbic acid, zingiber officinale (ginger) root extract, stearamidopropyl PG-dimonium chloride phosphate, butylene glycol, behenic acid, ceteareth-25, propylene glycol, ethylhexylglycerin, steareth-2, methylparaben, tocopheryl acetate, hydrolyzed collagen, EDTA, potassium hydroxide, caramel

Please keep carton as it contains important information.

Principal Display Panel

GOLD BOND®  
CRACKED FOOT
SKIN RELIEF

Net wt 0.75 oz (21 g)            

Principal Display Panel
GOLD BOND®  
CRACKED FOOT
SKIN RELIEF
Net wt 0.75 oz (21 g)

GOLD BOND MEDICATED CRACKED FOOT SKIN RELIEF 
petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0175
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM30 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
STEARETH-21 (UNII: 53J3F32P58)  
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)  
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)  
JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ALLANTOIN (UNII: 344S277G0Z)  
SHEA BUTTER (UNII: K49155WL9Y)  
CERAMIDE NP (UNII: 4370DF050B)  
CERAMIDE NG (UNII: C04977SRJ5)  
CERAMIDE EOS (UNII: CR0J8RN66K)  
CERAMIDE 1 (UNII: 5THT33P7X7)  
CERAMIDE AP (UNII: F1X8L2B00J)  
COCODIMONIUM HYDROXYPROPYL HYDROLYZED KERATIN (1000 MW) (UNII: 8V0I3U3HMO)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
BIOTIN (UNII: 6SO6U10H04)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
N-HEXANOYLSPHINGOSINE (UNII: 038753E78J)  
LEVOMENOL (UNII: 24WE03BX2T)  
3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)  
GINGER (UNII: C5529G5JPQ)  
STEARAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: W6000VEI5Y)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
BEHENIC ACID (UNII: H390488X0A)  
CETEARETH-25 (UNII: 8FA93U5T67)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
STEARETH-2 (UNII: V56DFE46J5)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
HYDROLYSED BOVINE COLLAGEN (ENZYMATIC; 3500 MW) (UNII: 5WE8P977RQ)  
EDETIC ACID (UNII: 9G34HU7RV0)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
CARAMEL (UNII: T9D99G2B1R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-0175-31 in 1 CARTON01/01/2021
121 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01601/01/2021
Labeler - Chattem, Inc. (003336013)

Revised: 10/2023
Document Id: df28f8ce-7953-4d34-a110-6672c642c417
Set id: 21dbfb33-574b-4b9b-beb1-8490d3e0614c
Version: 3
Effective Time: 20231030
 
Chattem, Inc.