FAMILY WELLNESS- diphenhydramine hydrochloride, zinc acetate cream 
Zhejiang Jingwei Pharmaceutical Co., Ltd.

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Drug Facts

Inactive Ingredients - cetyl alcohol, glycerol stearate,

laureth-23, methylparaben, mineral oil, petrolatum, propylene

glycol, propylparaben, stearic acid, stearyl alcohol, water

Active Ingredients

Diphenhydramine hydrochloride 2 %

Zinc acetate 0.1 %

Purpose

---Topical analgesic

---Skin protectant

Uses  for temporary relief from pain and itching associated

with insect bites, sunburn and minor skin irritations. Dries the

oozing and weeping of poison: -ivy -oak - sumac

Warnings

For external use only

Do not use

-over large areas of the body

-with any other product containing diphenhydramine,

including those taken orally

When using this product - avoid contact with eyes

Ask a doctor before use

-on chicken pox

-on measles

Stop use and ask a doctor if:

-symptoms last for more than 7 days

-the condition gets worse

-symptoms clear up and then occur again within a few days

Keep out of reach of children. If swallowed, get medical help

or contact a Poison Control Center right away.

Directions

-for adults and children over 2 years of age: apply to affected area

not more than 3 or 4 times per day

-children under 2 years of age: ask a doctor before use

Other information - store at room temperature 59 - 86 F (15 - 30 C)

Questions? 1-800-639-3803 Weekdays 9 AM to 4 PM EST

copy of label

FAMILY WELLNESS 
diphenhydramine hydrochloride, zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55621-007
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CETYL ALCOHOL (UNII: 936JST6JCN)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
LAURETH-23 (UNII: N72LMW566G)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MINERAL OIL (UNII: T5L8T28FGP)  
PETROLATUM (UNII: 4T6H12BN9U)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55621-007-011 in 1 BOX11/01/2013
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01711/01/2013
Labeler - Zhejiang Jingwei Pharmaceutical Co., Ltd. (530876549)

Revised: 10/2023
Document Id: 0882dc65-a451-daec-e063-6394a90a10ff
Set id: fefbe351-1cd9-4a2f-a43d-51e2c4eb180b
Version: 4
Effective Time: 20231024
 
Zhejiang Jingwei Pharmaceutical Co., Ltd.